A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690697



Internal ID18988978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20064069..20152671hg38UCSC Ensembl
Innerchr9:20064067..20152669hg19UCSC Ensembl
Innerchr9:20054067..20142669hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3888603
hg1988603
hg1888603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021647
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690697
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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