A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632882



Internal ID7019693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:82118294..82174415hg38UCSC Ensembl
Innerchr13:82118294..82174415hg38UCSC Ensembl
Outerchr13:82117794..82174915hg38UCSC Ensembl
chr13:82692429..82748550hg19UCSC Ensembl
Innerchr13:82692429..82748550hg19UCSC Ensembl
Outerchr13:82691929..82749050hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3856122
hg1956122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14820089, essv14820084, essv14820090, essv14820092, essv14820085, essv14820091, essv14820088, essv14820086, essv14820087, essv14820083
SamplesNA21110, HG03926, NA21115, HG04214, HG03780, HG03781, NA21102, NA21093, HG03989, HG03864
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632882
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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