A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626163



Internal ID6666312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44595130..44595842hg38UCSC Ensembl
Innerchr11:44595180..44595792hg38UCSC Ensembl
Outerchr11:44595066..44595906hg38UCSC Ensembl
chr11:44616680..44617392hg19UCSC Ensembl
Innerchr11:44616730..44617342hg19UCSC Ensembl
Outerchr11:44616616..44617456hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38713
hg19713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14116453, essv14116460, essv14116455, essv14116459, essv14116457, essv14116456, essv14116458, essv14116454, essv14116452
SamplesHG01986, HG03115, HG02888, HG03079, HG03583, HG01088, HG03028, HG03461, HG03410
Known GenesCD82
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626163
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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