A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524857



Internal ID15452150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180380626..180394445hg38UCSC Ensembl
Innerchr5:179807626..179821445hg19UCSC Ensembl
Innerchr5:179740232..179754051hg18UCSC Ensembl
Innerchr5:179740232..179754051hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3813820
hg1913820
hg1813820
hg1713820
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700860
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524857
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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