A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14869692



Internal ID4209862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97756753..97791298hg38UCSC Ensembl
Innerchr13:97756769..97791282hg38UCSC Ensembl
Outerchr13:97756737..97791314hg38UCSC Ensembl
chr13:98409007..98443552hg19UCSC Ensembl
Innerchr13:98409023..98443536hg19UCSC Ensembl
Outerchr13:98408991..98443568hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3834546
hg1934546
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633298
Supporting Variants
SamplesHG03789
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14869692
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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