A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631759



Internal ID7018568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35185729..35186455hg38UCSC Ensembl
Innerchr13:35185744..35186440hg38UCSC Ensembl
Outerchr13:35185714..35186470hg38UCSC Ensembl
chr13:35759866..35760592hg19UCSC Ensembl
Innerchr13:35759881..35760577hg19UCSC Ensembl
Outerchr13:35759851..35760607hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14688374, essv14688373, essv14688375
SamplesNA20891, HG01586, HG04211
Known GenesNBEA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631759
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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