A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003992



Internal ID18746523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68917..256048hg38UCSC Ensembl
Innerchr4:68809..249837hg19UCSC Ensembl
Innerchr4:58809..239837hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38187132
hg19181029
hg18181029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5065n100
Supporting Variantsnssv3616066, nssv3616065
Samples
Known GenesZNF595, ZNF718, ZNF876P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003992
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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