A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511729



Internal ID18463324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:131448229..131943719hg38UCSC Ensembl
Innerchr10:133246492..133757223hg19UCSC Ensembl
Innerchr10:133136482..133607213hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38495491
hg19510732
hg18470732
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050992
Supporting Variants
Samples
Known GenesFLJ46300, PPP2R2D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3511729
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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