A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3504201



Internal ID18802482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20214982..20237863hg38UCSC Ensembl
Innerchr10:20503911..20526792hg19UCSC Ensembl
Innerchr10:20543917..20566798hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3822882
hg1922882
hg1822882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035861
Supporting Variants
Samples
Known GenesPLXDC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3504201
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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