A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013934



Internal ID18756466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35822..150780hg38UCSC Ensembl
Innerchr4:35822..144564hg19UCSC Ensembl
Innerchr4:25822..134564hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38114959
hg19108743
hg18108743
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3615267
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)nsv1013934
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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