A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689162



Internal ID15079128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30598866..30654632hg38UCSC Ensembl
Innerchr9:30598864..30654630hg19UCSC Ensembl
Innerchr9:30588864..30644630hg18UCSC Ensembl
Innerchr9:30588864..30644630hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3855767
hg1955767
hg1855767
hg1755767
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517063
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689162
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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