A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519778



Internal ID15100385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:476854..490122hg38UCSC Ensembl
Innerchr5:476969..490237hg19UCSC Ensembl
Innerchr5:529969..543237hg18UCSC Ensembl
Innerchr5:529969..543237hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3813269
hg1913269
hg1813269
hg1713269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv691336, nssv658512
Samples
Known GenesSLC9A3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519778
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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