A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5795576



Internal ID8772979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96351365..96362433hg38UCSC Ensembl
Outerchr13:96351328..96362483hg38UCSC Ensembl
Innerchr13:97003619..97014687hg19UCSC Ensembl
Outerchr13:97003582..97014737hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3811156
hg1911156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678219
Supporting Variants
SamplesNA19717
Known GenesHS6ST3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5795576
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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