A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628108



Internal ID6668252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131630105..131630632hg38UCSC Ensembl
Innerchr11:131630105..131630632hg38UCSC Ensembl
Outerchr11:131629827..131630889hg38UCSC Ensembl
chr11:131499999..131500526hg19UCSC Ensembl
Innerchr11:131499999..131500526hg19UCSC Ensembl
Outerchr11:131499721..131500783hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14316960, essv14316957, essv14316955, essv14316959, essv14316958, essv14316953, essv14316954, essv14316952, essv14316961, essv14316956
SamplesNA18874, NA18993, NA18973, HG00662, HG02840, NA19080, NA18923, NA18853, NA19065, HG03091
Known GenesNTM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628108
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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