A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3737942



Internal ID18689537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..62222hg38UCSC Ensembl
Innerchr4:12269..62114hg19UCSC Ensembl
Innerchr4:2269..52114hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3849954
hg1949846
hg1849846
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006094
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)nssv3737942
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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