A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518472



Internal ID15099079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2346678..2515720hg38UCSC Ensembl
Innerchr4:2348405..2517447hg19UCSC Ensembl
Innerchr4:2318203..2487245hg18UCSC Ensembl
Innerchr4:2315636..2484678hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38169043
hg19169043
hg18169043
hg17169043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695908
Samples
Known GenesLOC402160, RNF4, ZFYVE28
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518472
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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