A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3496094



Internal ID18737049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2651106..3081241hg38UCSC Ensembl
Innerchr10:2693298..3123433hg19UCSC Ensembl
Innerchr10:2683298..3113433hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38430136
hg19430136
hg18430136
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054918
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)nssv3496094
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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