A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526798



Internal ID15107405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:130774027..130994774hg38UCSC Ensembl
Innerchr5:130109720..130330467hg19UCSC Ensembl
Innerchr5:130137619..130358366hg18UCSC Ensembl
Innerchr5:130137619..130358366hg17UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg38220748
hg19220748
hg18220748
hg17220748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703152
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526798
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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