A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525645



Internal ID15452938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:71595735..71601874hg38UCSC Ensembl
Innerchr4:72461452..72467591hg19UCSC Ensembl
Innerchr4:72680316..72686455hg18UCSC Ensembl
Innerchr4:72826487..72832626hg17UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg386140
hg196140
hg186140
hg176140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701799
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525645
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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