A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011039



Internal ID18753572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68917..335897hg38UCSC Ensembl
Innerchr4:68809..329686hg19UCSC Ensembl
Innerchr4:58809..319686hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38266981
hg19260878
hg18260878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3738091
Samples
Known GenesZNF595, ZNF718, ZNF732, ZNF876P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011039
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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