A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517733



Internal ID15445026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:23636476..23729264hg38UCSC Ensembl
Innerchr4:23638099..23730887hg19UCSC Ensembl
Innerchr4:23247197..23339985hg18UCSC Ensembl
Innerchr4:23314368..23407156hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3892789
hg1992789
hg1892789
hg1792789
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv682000, nssv656983, nssv677877, nssv653039
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517733
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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