A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001177



Internal ID18743708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..71528hg38UCSC Ensembl
Innerchr4:12269..71420hg19UCSC Ensembl
Innerchr4:2269..61420hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3859260
hg1959152
hg1859152
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5056n100
Supporting Variantsnssv3615148
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)nsv1001177
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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