A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691983



Internal ID18990264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25260928..25353889hg38UCSC Ensembl
Innerchr9:25260926..25353887hg19UCSC Ensembl
Innerchr9:25250926..25343887hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3892962
hg1992962
hg1892962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032258
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)nssv3691983
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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