A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521588



Internal ID15448881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:119672720..119680118hg38UCSC Ensembl
Innerchr5:119008415..119015813hg19UCSC Ensembl
Innerchr5:119036314..119043712hg18UCSC Ensembl
Innerchr5:119036314..119043712hg17UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg387399
hg197399
hg187399
hg177399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv352n21
Supporting Variantsnssv698206
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521588
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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