A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528056



Internal ID15108663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:98382257..98598992hg38UCSC Ensembl
Innerchr3:98101101..98317836hg19UCSC Ensembl
Innerchr3:99583791..99800526hg18UCSC Ensembl
Innerchr3:99583791..99800526hg17UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38216736
hg19216736
hg18216736
hg17216736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv293n21
Supporting Variantsnssv704590
Samples
Known GenesCLDND1, CPOX, GPR15, OR5K1, OR5K2, OR5K3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528056
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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