A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646969



Internal ID7033711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36327319..36327848hg38UCSC Ensembl
Innerchr21:36327320..36327848hg38UCSC Ensembl
Outerchr21:36327319..36327849hg38UCSC Ensembl
chr21:37699617..37700146hg19UCSC Ensembl
Innerchr21:37699618..37700146hg19UCSC Ensembl
Outerchr21:37699617..37700147hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38530
hg19530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16319476, essv16319533, essv16319471, essv16319508, essv16319524, essv16319489, essv16319521, essv16319455, essv16319547, essv16319484, essv16319514, essv16319485, essv16319461, essv16319529, essv16319448, essv16319467, essv16319543, essv16319506, essv16319492, essv16319480, essv16319466, essv16319503, essv16319556, essv16319542, essv16319479, essv16319550, essv16319497, essv16319491, essv16319510, essv16319530, essv16319487, essv16319483, essv16319552, essv16319549, essv16319452, essv16319532, essv16319464, essv16319486, essv16319468, essv16319490, essv16319478, essv16319463, essv16319482, essv16319458, essv16319473, essv16319494, essv16319554, essv16319496, essv16319500, essv16319470, essv16319545, essv16319540, essv16319531, essv16319517, essv16319528, essv16319522, essv16319495, essv16319546, essv16319535, essv16319481, essv16319509, essv16319474, essv16319504, essv16319518, essv16319538, essv16319488, essv16319450, essv16319539, essv16319453, essv16319553, essv16319548, essv16319477, essv16319472, essv16319525, essv16319537, essv16319501, essv16319454, essv16319459, essv16319534, essv16319536, essv16319511, essv16319493, essv16319498, essv16319558, essv16319544, essv16319475, essv16319460, essv16319512, essv16319457, essv16319505, essv16319502, essv16319520, essv16319551, essv16319527, essv16319515, essv16319519, essv16319513, essv16319469, essv16319523, essv16319456, essv16319449, essv16319447, essv16319555, essv16319541, essv16319526, essv16319516, essv16319499, essv16319462, essv16319557, essv16319507, essv16319465, essv16319451
SamplesHG01986, HG02574, NA19028, HG03484, NA18508, HG03517, HG02798, NA19020, HG02012, HG02624, HG03297, HG02888, HG02589, HG01051, NA20356, NA19314, HG03478, HG03436, NA20320, HG03091, NA18916, NA19138, NA19904, HG02505, HG02703, HG02315, HG03268, HG02634, NA19917, NA19207, NA20412, HG02545, NA20355, NA20342, NA19209, HG03369, NA20318, HG03048, HG02819, HG02479, HG03120, HG02570, NA19437, HG03160, HG03132, HG03363, NA19707, HG03061, HG03511, HG01104, HG03547, NA19184, HG02108, NA19236, NA19982, HG03575, NA20126, NA18910, NA18871, HG03124, HG03563, HG03085, NA19114, NA19118, HG03446, HG02884, HG02309, NA19099, HG03451, HG02666, HG02332, NA19625, HG02568, HG02484, HG02722, HG03567, HG02255, HG02613, NA19309, HG02282, HG03367, NA20276, HG02983, HG01894, HG01915, NA19380, NA19144, NA19360, HG02814, HG02558, HG03084, NA19117, NA19223, HG03066, HG03313, HG03049, HG03279, HG03258, NA20289, HG02768, HG02676, NA18873, NA18876, HG03445, HG02763, HG02855, NA18488, HG02851, HG02808, HG03303, HG03166, HG03265
Known GenesMORC3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646969
Frequency
Sample Size2504
Observed Gain0
Observed Loss112
Observed Complex0
Frequencyn/a


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