A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042698



Internal ID18785229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2645902..3076679hg38UCSC Ensembl
Innerchr10:2688094..3118871hg19UCSC Ensembl
Innerchr10:2678094..3108871hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38430778
hg19430778
hg18430778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv660n100
Supporting Variantsnssv3499759
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)nsv1042698
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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