A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633269



Internal ID6673391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96351336..96362482hg38UCSC Ensembl
Innerchr13:96351336..96362482hg38UCSC Ensembl
Outerchr13:96351144..96362756hg38UCSC Ensembl
chr13:97003590..97014736hg19UCSC Ensembl
Innerchr13:97003590..97014736hg19UCSC Ensembl
Outerchr13:97003398..97015010hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3811147
hg1911147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14869321
SamplesNA19717
Known GenesHS6ST3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633269
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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