A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13573124



Internal ID3802105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96733041..96742906hg38UCSC Ensembl
Innerchr9:96733191..96742756hg38UCSC Ensembl
Outerchr9:96732891..96743056hg38UCSC Ensembl
chr9:99495323..99505188hg19UCSC Ensembl
Innerchr9:99495473..99505038hg19UCSC Ensembl
Outerchr9:99495173..99505338hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg389866
hg199866
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621171
Supporting Variants
SamplesHG03446
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13573124
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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