A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3497286



Internal ID19084927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:233716299..233811039hg38UCSC Ensembl
Innerchr1:233852045..233946785hg19UCSC Ensembl
Innerchr1:231918668..232013408hg18UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3894741
hg1994741
hg1894741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013472
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)nssv3497286
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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