A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518567



Internal ID15445860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:170182185..170199025hg38UCSC Ensembl
Innerchr4:171103336..171120176hg19UCSC Ensembl
Innerchr4:171339911..171356751hg18UCSC Ensembl
Innerchr4:171478066..171494906hg17UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3816841
hg1916841
hg1816841
hg1716841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696010
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518567
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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