A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666299



Internal ID9932404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24722287..24724493hg38UCSC Ensembl
Outerchr10:24721916..24724863hg38UCSC Ensembl
Innerchr10:25011216..25013422hg19UCSC Ensembl
Outerchr10:25010845..25013792hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg382948
hg192948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5891395, essv6567349, essv6097634, essv5598023, essv6092662, essv5588828, essv6474815, essv5498232, essv5507464, essv5620189, essv5982111, essv6506409, essv5501409, essv6069257, essv5810148, essv6363673, essv5889129, essv5629672, essv6483503, essv6473962, essv6372109, essv5970724, essv5951295, essv6362301, essv5491417, essv5803966, essv6496896, essv6332695, essv5675191, essv5397330, essv6455206, essv5926456, essv5535388, essv5465130, essv5609370, essv6411916, essv6039874, essv5941832, essv5897451, essv6547125, essv6218153, essv6523097, essv6156509, essv6372661, essv5395646, essv5689193, essv6342447, essv5405837, essv6055365, essv5460951, essv6462381, essv6120438, essv5645953, essv6498861, essv5489511, essv5721211, essv5667025, essv6423060, essv5685159, essv6170069, essv6485769, essv5871714, essv6374215, essv5592435, essv6181204, essv5558822, essv5766140, essv5860413, essv5452407, essv6066967, essv6414598, essv6261207, essv5899322, essv6154510, essv5458640, essv5701869, essv6509176, essv6510535
SamplesHG00403, HG00650, HG00542, HG00442, HG00608, HG00671, HG00524, HG00699, HG00449, HG00654, HG00693, HG00589, HG00501, HG00702, HG00689, HG00448, HG00634, HG00610, HG00537, HG00590, HG00512, HG00683, HG00534, HG00422, HG00705, HG00427, HG00530, HG00419, HG00464, HG00543, HG00629, HG00443, HG00596, HG00428, HG00653, HG00701, HG00657, HG00475, HG00436, HG00556, HG00584, HG00533, HG00583, HG00500, HG00619, HG00708, HG00635, HG00651, HG00404, HG00531, HG00479, HG00684, HG00613, HG00525, HG00704, HG00611, HG00476, HG00625, HG00565, HG00473, HG00607, HG00662, HG00620, HG00707, HG00672, HG00614, HG00513, HG00578, HG00478, HG00421, HG00656, HG00698, HG00595, HG00472, HG00628, HG00437, HG00581, HG00593
Known GenesARHGAP21
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666299
Frequency
Sample Size1151
Observed Gain0
Observed Loss78
Observed Complex0
Frequencyn/a


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