A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691995



Internal ID18990276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26265536..26434484hg38UCSC Ensembl
Innerchr9:26265534..26434482hg19UCSC Ensembl
Innerchr9:26255534..26424482hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38168949
hg19168949
hg18168949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016727
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)nssv3691995
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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