A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696484



Internal ID15433136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:73173740..73213791hg38UCSC Ensembl
Innerchr9:75788656..75828707hg19UCSC Ensembl
Innerchr9:74978476..75018527hg18UCSC Ensembl
Innerchr9:73018210..73058261hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3840052
hg1940052
hg1840052
hg1740052
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519016
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696484
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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