A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703513



Internal ID15440165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33465653..33467597hg38UCSC Ensembl
Innerchr9:33465651..33467595hg19UCSC Ensembl
Innerchr9:33455651..33457595hg18UCSC Ensembl
Innerchr9:33455651..33457595hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381945
hg191945
hg181945
hg171945
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527128
Supporting Variants
Samples
Known GenesNOL6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703513
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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