A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690696



Internal ID18988977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20013894..20067332hg38UCSC Ensembl
Innerchr9:20013892..20067330hg19UCSC Ensembl
Innerchr9:20003892..20057330hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3853439
hg1953439
hg1853439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028297
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)nssv3690696
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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