A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009916



Internal ID19099135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:44292161..44382775hg38UCSC Ensembl
Innerchr4:44294178..44384792hg19UCSC Ensembl
Innerchr4:43988935..44079549hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3890615
hg1990615
hg1890615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625053
Samples
Known GenesKCTD8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009916
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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