A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663270



Internal ID15053236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30403519..30558224hg38UCSC Ensembl
Innerchr9:30403517..30558222hg19UCSC Ensembl
Innerchr9:30393517..30548222hg18UCSC Ensembl
Innerchr9:30393517..30548222hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38154706
hg19154706
hg18154706
hg17154706
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517063
Supporting Variants
Samples
Known GenesLOC401497
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663270
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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