A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664885



Internal ID15401537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111123414..111129108hg38UCSC Ensembl
Innerchr9:113885694..113891388hg19UCSC Ensembl
Innerchr9:112925515..112931209hg18UCSC Ensembl
Innerchr9:110965249..110970943hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg385695
hg195695
hg185695
hg175695
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517160
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664885
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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