A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3615194



Internal ID18913475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..94493hg38UCSC Ensembl
Innerchr4:12269..94380hg19UCSC Ensembl
Innerchr4:2269..84380hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3882225
hg1982112
hg1882112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002614
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)nssv3615194
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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