A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3626029



Internal ID18924310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:65726020..65767127hg38UCSC Ensembl
Innerchr4:66591738..66632845hg19UCSC Ensembl
Innerchr4:66274333..66315440hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3841108
hg1941108
hg1841108
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003147
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)nssv3626029
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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