A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3490639



Internal ID18731594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2649384..3091891hg38UCSC Ensembl
Innerchr10:2691576..3134083hg19UCSC Ensembl
Innerchr10:2681576..3124083hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38442508
hg19442508
hg18442508
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044605
Supporting Variants
Samples
Known GenesPFKP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3490639
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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