A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523377



Internal ID15450670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25992348..26013192hg38UCSC Ensembl
Innerchr5:25992457..26013301hg19UCSC Ensembl
Innerchr5:26028214..26049058hg18UCSC Ensembl
Innerchr5:26028214..26049058hg17UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3820845
hg1920845
hg1820845
hg1720845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699126
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523377
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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