A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631531



Internal ID7018340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:23718767..23811145hg38UCSC Ensembl
Innerchr13:23718775..23811137hg38UCSC Ensembl
Outerchr13:23718759..23811153hg38UCSC Ensembl
chr13:24292906..24385284hg19UCSC Ensembl
Innerchr13:24292914..24385276hg19UCSC Ensembl
Outerchr13:24292898..24385292hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3892379
hg1992379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14669711
SamplesNA18559
Known GenesMIPEP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631531
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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