A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519787



Internal ID15447080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192881547..192895132hg38UCSC Ensembl
Innerchr3:192599336..192612921hg19UCSC Ensembl
Innerchr3:194082030..194095615hg18UCSC Ensembl
Innerchr3:194082038..194095623hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3813586
hg1913586
hg1813586
hg1713586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv308n21
Supporting Variantsnssv697051
Samples
Known GenesMB21D2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519787
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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