A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005940



Internal ID18748471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..158587hg38UCSC Ensembl
Innerchr4:12269..152378hg19UCSC Ensembl
Innerchr4:2269..142378hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38146319
hg19140110
hg18140110
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5060n100
Supporting Variantsnssv3615215
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)nsv1005940
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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