A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3615182



Internal ID18913463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..85265hg38UCSC Ensembl
Innerchr4:12269..85156hg19UCSC Ensembl
Innerchr4:2269..75156hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3872997
hg1972888
hg1872888
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002019
Supporting Variants
Samples
Known GenesZNF595, ZNF718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3615182
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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