A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662324



Internal ID9928429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107365790..107373396hg38UCSC Ensembl
Outerchr11:107365419..107373766hg38UCSC Ensembl
Innerchr11:107236516..107244122hg19UCSC Ensembl
Outerchr11:107236145..107244492hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg388348
hg198348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv239e199
Supporting Variantsessv6287627, essv5944471, essv6209113, essv6167722, essv6384694, essv5862382, essv6347116, essv6334740, essv6521972, essv5851061, essv5546878, essv5693220, essv6377920, essv5937583, essv5513732, essv6459570, essv6307889
SamplesHG01356, HG01462, HG01359, HG01374, HG01461, HG01366, HG01134, HG01455, HG01550, HG01136, HG01360, HG01384, HG01390, HG01375, HG01342, HG01125, HG01437
Known GenesCWF19L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662324
Frequency
Sample Size1151
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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