A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639413



Internal ID18937694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:125553142..125667828hg38UCSC Ensembl
Innerchr4:126474297..126588983hg19UCSC Ensembl
Innerchr4:126693747..126808433hg18UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38114687
hg19114687
hg18114687
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003442
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)nssv3639413
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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