A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677997



Internal ID15067963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30647720..30733388hg38UCSC Ensembl
Innerchr9:30647718..30733386hg19UCSC Ensembl
Innerchr9:30637718..30723386hg18UCSC Ensembl
Innerchr9:30637718..30723386hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3885669
hg1985669
hg1885669
hg1785669
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)nssv677997
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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