A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13526632



Internal ID3982540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75190493..75199089hg38UCSC Ensembl
Innerchr9:75190493..75199089hg38UCSC Ensembl
Outerchr9:75190343..75199322hg38UCSC Ensembl
chr9:77805409..77814005hg19UCSC Ensembl
Innerchr9:77805409..77814005hg19UCSC Ensembl
Outerchr9:77805259..77814238hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg388597
hg198597
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620716
Supporting Variants
SamplesHG03636
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13526632
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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