A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647901



Internal ID7034640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44535057..44536020hg38UCSC Ensembl
Innerchr22:44535057..44536020hg38UCSC Ensembl
Outerchr22:44534783..44536304hg38UCSC Ensembl
chr22:44930937..44931900hg19UCSC Ensembl
Innerchr22:44930937..44931900hg19UCSC Ensembl
Outerchr22:44930663..44932184hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38964
hg19964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16437581, essv16437541, essv16437523, essv16437528, essv16437587, essv16437569, essv16437500, essv16437575, essv16437554, essv16437577, essv16437573, essv16437492, essv16437507, essv16437580, essv16437557, essv16437513, essv16437534, essv16437497, essv16437516, essv16437545, essv16437490, essv16437547, essv16437510, essv16437526, essv16437502, essv16437496, essv16437533, essv16437562, essv16437522, essv16437493, essv16437555, essv16437576, essv16437501, essv16437542, essv16437553, essv16437551, essv16437527, essv16437578, essv16437519, essv16437537, essv16437543, essv16437506, essv16437487, essv16437503, essv16437565, essv16437529, essv16437508, essv16437556, essv16437509, essv16437566, essv16437495, essv16437489, essv16437548, essv16437546, essv16437563, essv16437512, essv16437550, essv16437582, essv16437574, essv16437572, essv16437517, essv16437571, essv16437564, essv16437504, essv16437520, essv16437586, essv16437511, essv16437579, essv16437494, essv16437488, essv16437540, essv16437539, essv16437583, essv16437585, essv16437538, essv16437559, essv16437567, essv16437531, essv16437505, essv16437498, essv16437535, essv16437584, essv16437536, essv16437558, essv16437532, essv16437499, essv16437530, essv16437491, essv16437560, essv16437544, essv16437568, essv16437514, essv16437518, essv16437524, essv16437561, essv16437552, essv16437521, essv16437549, essv16437515, essv16437570, essv16437525
SamplesHG01985, HG02339, HG02890, HG03484, HG02583, NA19909, HG03052, NA19204, NA19914, NA18877, NA20298, HG03100, HG03295, HG03139, HG02888, HG01051, NA19920, NA20359, NA19107, HG03095, HG03572, HG02621, HG02811, HG03135, HG03091, HG02325, NA19198, NA20317, NA18916, NA19197, HG03105, HG02981, HG03209, HG02562, HG03520, HG02703, HG02315, NA19238, NA19024, NA19317, HG02471, HG02502, NA18520, HG03073, HG01550, NA19247, NA19437, HG03061, HG01247, HG03088, HG02334, NA19175, NA19236, HG02322, HG02450, HG03428, HG02497, HG02878, HG03294, HG01390, HG03123, HG02577, HG03397, NA18912, HG03446, HG02881, HG03024, HG03391, HG03046, HG02585, HG01403, NA18523, HG03354, NA19160, HG02635, HG02484, HG02722, NA19035, HG03064, HG02455, NA19390, HG02759, HG02308, HG01958, HG02923, HG02837, HG02611, HG02314, HG03259, HG03469, NA20281, HG03084, HG03432, NA19223, HG03049, NA19474, HG03351, HG02676, HG03445, HG02763, HG02643
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647901
Frequency
Sample Size2504
Observed Gain0
Observed Loss101
Observed Complex0
Frequencyn/a


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