A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632964



Internal ID7019774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:84973610..84981465hg38UCSC Ensembl
Innerchr13:84973610..84981465hg38UCSC Ensembl
Outerchr13:84973110..84981965hg38UCSC Ensembl
chr13:85547745..85555600hg19UCSC Ensembl
Innerchr13:85547745..85555600hg19UCSC Ensembl
Outerchr13:85547245..85556100hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg387856
hg197856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14822757, essv14822756
SamplesNA18990, NA18991
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632964
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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