A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692372



Internal ID18990653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:3743276..3757758hg38UCSC Ensembl
Innerchr9:3743276..3757758hg19UCSC Ensembl
Innerchr9:3733276..3747758hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3814483
hg1914483
hg1814483
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018948
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)nssv3692372
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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