A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632775



Internal ID7019586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77391686..77398964hg38UCSC Ensembl
Innerchr13:77391686..77398964hg38UCSC Ensembl
Outerchr13:77391457..77399193hg38UCSC Ensembl
chr13:77965821..77973099hg19UCSC Ensembl
Innerchr13:77965821..77973099hg19UCSC Ensembl
Outerchr13:77965592..77973328hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg387279
hg197279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14800948, essv14800952, essv14800954, essv14800949, essv14800950, essv14800953, essv14800951, essv14800956, essv14800955
SamplesHG02804, HG01500, HG03370, NA19917, HG03120, HG02144, HG03159, HG01392, HG02586
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632775
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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