A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631791



Internal ID7018600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36923192..36926599hg38UCSC Ensembl
Innerchr13:36923192..36926599hg38UCSC Ensembl
Outerchr13:36922927..36926870hg38UCSC Ensembl
chr13:37497329..37500736hg19UCSC Ensembl
Innerchr13:37497329..37500736hg19UCSC Ensembl
Outerchr13:37497064..37501007hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg383408
hg193408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14693752, essv14693751, essv14693749, essv14693750, essv14693753
SamplesHG00361, HG00369, HG00332, HG00324, HG00342
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631791
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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