A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631700



Internal ID7018508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31581557..31632548hg38UCSC Ensembl
Innerchr13:31581557..31632548hg38UCSC Ensembl
Outerchr13:31581057..31633048hg38UCSC Ensembl
chr13:32155694..32206685hg19UCSC Ensembl
Innerchr13:32155694..32206685hg19UCSC Ensembl
Outerchr13:32155194..32207185hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3850992
hg1950992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14683344, essv14683342, essv14683343
SamplesHG01398, HG01396, HG01089
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631700
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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