A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585506



Internal ID6973029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24569283..24574380hg38UCSC Ensembl
Innerchr1:24569283..24574380hg38UCSC Ensembl
Outerchr1:24568921..24574877hg38UCSC Ensembl
chr1:24895774..24900871hg19UCSC Ensembl
Innerchr1:24895774..24900871hg19UCSC Ensembl
Outerchr1:24895412..24901368hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385098
hg195098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9891531, essv9891502, essv9891553, essv9891534, essv9891543, essv9891546, essv9891469, essv9891489, essv9891560, essv9891586, essv9891496, essv9891480, essv9891467, essv9891511, essv9891486, essv9891523, essv9891569, essv9891550, essv9891459, essv9891570, essv9891547, essv9891464, essv9891527, essv9891508, essv9891581, essv9891473, essv9891522, essv9891457, essv9891554, essv9891483, essv9891565, essv9891528, essv9891519, essv9891562, essv9891583, essv9891533, essv9891455, essv9891506, essv9891582, essv9891505, essv9891557, essv9891566, essv9891481, essv9891577, essv9891590, essv9891538, essv9891563, essv9891589, essv9891541, essv9891470, essv9891493, essv9891544, essv9891558, essv9891504, essv9891463, essv9891460, essv9891490, essv9891573, essv9891564, essv9891518, essv9891525, essv9891501, essv9891477, essv9891575, essv9891548, essv9891485, essv9891576, essv9891567, essv9891551, essv9891532, essv9891574, essv9891510, essv9891515, essv9891584, essv9891561, essv9891462, essv9891499, essv9891588, essv9891555, essv9891578, essv9891476, essv9891495, essv9891585, essv9891468, essv9891552, essv9891482, essv9891568, essv9891537, essv9891520, essv9891591, essv9891458, essv9891521, essv9891488, essv9891580, essv9891479, essv9891536, essv9891512, essv9891492, essv9891484, essv9891526, essv9891535, essv9891503, essv9891456, essv9891556, essv9891497, essv9891461, essv9891500, essv9891524, essv9891466, essv9891571, essv9891572, essv9891579, essv9891545, essv9891509, essv9891514, essv9891516, essv9891454, essv9891507, essv9891474, essv9891549, essv9891472, essv9891494, essv9891491, essv9891487, essv9891517, essv9891542, essv9891530, essv9891498, essv9891587, essv9891540, essv9891475, essv9891529, essv9891465, essv9891513, essv9891471, essv9891539, essv9891559, essv9891478
SamplesNA19222, HG02496, HG01098, NA18924, NA19466, NA19204, NA18508, HG01885, NA19704, HG02419, HG03115, NA18486, HG03521, HG03298, NA20294, HG03515, HG03139, HG02589, NA19098, HG03069, NA19446, HG03074, HG03135, NA18923, HG02756, HG03105, NA19457, HG02054, NA18498, HG03224, HG02505, HG02281, HG02562, HG03189, NA18874, HG02573, NA19917, NA19372, NA19235, NA19207, NA19172, HG02420, HG02571, HG03380, HG02502, NA19189, NA18864, HG03055, HG03394, HG02882, HG02879, HG02977, HG02439, NA19908, NA19210, HG03132, HG03363, HG03061, HG03088, NA18933, HG02678, HG02511, HG01879, NA19913, HG02554, HG02144, HG02953, HG01989, NA20126, NA18910, HG02968, HG02102, HG02976, HG02537, HG03294, HG01390, NA19654, HG03563, HG03472, HG03301, HG03085, NA18879, NA19449, HG03202, HG03388, HG03078, NA18912, HG02309, NA18853, HG03571, HG03024, NA20282, HG01286, NA19395, HG01956, NA19436, HG02813, HG02613, NA19206, HG03240, NA19834, NA19149, HG02501, HG01551, NA19331, HG01958, NA19334, HG03259, HG03469, HG03304, HG02839, HG02580, HG02317, HG02558, HG03084, NA20357, NA20348, HG03097, HG02646, HG03049, HG03279, HG02938, NA19185, NA19711, HG03538, HG01883, NA19121, HG02947, NA18505, HG02855, NA19316, HG02851, NA18511, HG01886, NA18522, HG02808, HG03166, HG02760
Known GenesNCMAP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585506
Frequency
Sample Size2504
Observed Gain0
Observed Loss138
Observed Complex0
Frequencyn/a


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