A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3612694



Internal ID18910975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:166460712..166965620hg38UCSC Ensembl
Innerchr3:166178500..166683408hg19UCSC Ensembl
Innerchr3:167661194..168166102hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38504909
hg19504909
hg18504909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002090
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)nssv3612694
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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