A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664222



Internal ID9930327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97988636..97993092hg38UCSC Ensembl
Outerchr15:97988265..97993462hg38UCSC Ensembl
Innerchr15:98531866..98536322hg19UCSC Ensembl
Outerchr15:98531495..98536692hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg385198
hg195198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv469e199
Supporting Variantsessv5917898, essv5608243, essv6167462, essv5660569, essv6136883, essv6516810, essv5789832, essv6360723, essv6181773, essv6240272, essv5600358, essv6423315, essv5449070, essv6306684, essv6092506, essv5730605, essv5609943, essv5530750, essv6590737, essv6501733, essv6503570, essv6136691, essv6362675, essv6149954, essv5806285, essv6403747, essv5405104
SamplesNA18502, NA18861, NA18486, NA18504, NA18870, NA19171, NA19119, NA19197, NA18868, NA19137, NA19172, NA19209, NA18934, NA19152, NA18910, NA19114, NA18856, NA19225, NA18523, NA18909, NA19108, NA19093, NA19213, NA19129, NA18511, NA18522, NA19153
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664222
Frequency
Sample Size1151
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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