A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519138



Internal ID15446431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:109479380..109480877hg38UCSC Ensembl
Innerchr5:108815081..108816578hg19UCSC Ensembl
Innerchr5:108842980..108844477hg18UCSC Ensembl
Innerchr5:108842980..108844477hg17UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg381498
hg191498
hg181498
hg171498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696616
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519138
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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