A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3744272



Internal ID19042553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:156690847..156740998hg38UCSC Ensembl
Innerchr4:157611999..157662150hg19UCSC Ensembl
Innerchr4:157831449..157881600hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3850152
hg1950152
hg1850152
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028810
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)nssv3744272
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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