A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690744



Internal ID18989025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23927057..24048928hg38UCSC Ensembl
Innerchr9:23927055..24048926hg19UCSC Ensembl
Innerchr9:23917055..24038926hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38121872
hg19121872
hg18121872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027636
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)nssv3690744
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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