A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674741



Internal ID9940846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66517228..66518284hg38UCSC Ensembl
Outerchr15:66516857..66518654hg38UCSC Ensembl
Innerchr15:66809566..66810622hg19UCSC Ensembl
Outerchr15:66809195..66810992hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381798
hg191798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6312872, essv5402908, essv6463534, essv6436845, essv5571765, essv6566661, essv5638620, essv6319655, essv6013929, essv5801142, essv5478460, essv6013721, essv5464711, essv5640552, essv6489091, essv6330002, essv5960915, essv6232809, essv6359640, essv5924853, essv6333945, essv6417368, essv6566723, essv5680106, essv5684189, essv5770362, essv5629259, essv5497739, essv6505197, essv6174556, essv5606269, essv5635136, essv5459300, essv6093372, essv6326006, essv5705826, essv5441667, essv6556199, essv5549313, essv6080380, essv6060268, essv5530922, essv6159441, essv5397181, essv5679473, essv5601198, essv5863476, essv5527035, essv6533371, essv6226471, essv6408147, essv6328789, essv6175244, essv6016342, essv6463109, essv6267226, essv6170411, essv5542630, essv5404649, essv6166555, essv6201162, essv6178780, essv6259642, essv6370135, essv5933995, essv6289067, essv5991495, essv6389904, essv6583052, essv6477816, essv5810648
SamplesHG00403, HG00650, HG00542, HG00442, HG00592, HG00608, HG00559, HG00699, HG00566, HG00449, HG00654, HG00663, HG00589, HG00501, HG00702, HG00537, HG00590, HG00512, HG00683, HG00534, HG00705, HG00427, HG00530, HG00419, HG00464, HG00560, HG00629, HG00596, HG00557, HG00428, HG00653, HG00577, HG00701, HG00475, HG00436, HG00584, HG00533, HG00583, HG00500, HG00619, HG00708, HG00692, HG00651, HG00690, HG00404, HG00531, HG00684, HG00525, HG00704, HG00463, HG00611, HG00476, HG00625, HG00565, HG00473, HG00607, HG00418, HG00620, HG00707, HG00672, HG00614, HG00513, HG00578, HG00478, HG00656, HG00698, HG00472, HG00628, HG00437, HG00581, HG00593
Known GenesZWILCH
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674741
Frequency
Sample Size1151
Observed Gain0
Observed Loss71
Observed Complex0
Frequencyn/a


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