A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009336



Internal ID18751867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:273074..481679hg38UCSC Ensembl
Innerchr4:266863..475468hg19UCSC Ensembl
Innerchr4:256863..465468hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38208606
hg19208606
hg18208606
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3738101
Samples
Known GenesABCA11P, ZNF141, ZNF721, ZNF732
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009336
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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