A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3738462



Internal ID19036743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:193149584..193165102hg38UCSC Ensembl
Innerchr3:192867373..192882891hg19UCSC Ensembl
Innerchr3:194350067..194365585hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3815519
hg1915519
hg1815519
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007407
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)nssv3738462
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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