A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000704



Internal ID18743235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68917..207945hg38UCSC Ensembl
Innerchr4:68809..201734hg19UCSC Ensembl
Innerchr4:58809..191734hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38139029
hg19132926
hg18132926
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5070n100
Supporting Variantsnssv3616064
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)nsv1000704
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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