A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043848



Internal ID18786379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2645902..3091891hg38UCSC Ensembl
Innerchr10:2688094..3134083hg19UCSC Ensembl
Innerchr10:2678094..3124083hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38445990
hg19445990
hg18445990
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv660n100
Supporting Variantsnssv3501525, nssv3488225
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)nsv1043848
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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