A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005529



Internal ID18748060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34614..66074hg38UCSC Ensembl
Innerchr4:34614..65966hg19UCSC Ensembl
Innerchr4:24614..55966hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3831461
hg1931353
hg1831353
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5066n100
Supporting Variantsnssv3615260, nssv3738061, nssv3615261
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)nsv1005529
Frequency
Sample Size29084
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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