A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521454



Internal ID15448747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:79677642..79732866hg38UCSC Ensembl
Innerchr4:80598796..80654020hg19UCSC Ensembl
Innerchr4:80817820..80873044hg18UCSC Ensembl
Innerchr4:80955975..81011199hg17UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3855225
hg1955225
hg1855225
hg1755225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698065
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521454
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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