A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3615176



Internal ID18566771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..84076hg38UCSC Ensembl
Innerchr4:12269..83967hg19UCSC Ensembl
Innerchr4:2269..73967hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3871808
hg1971699
hg1871699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006251
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)nssv3615176
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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