A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3607947



Internal ID18906228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162343991..162438955hg38UCSC Ensembl
Innerchr3:162061779..162156743hg19UCSC Ensembl
Innerchr3:163544473..163639437hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3894965
hg1994965
hg1894965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002279
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)nssv3607947
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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