A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043925



Internal ID18786456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:128040003..128445808hg38UCSC Ensembl
Innerchr10:129838267..130244072hg19UCSC Ensembl
Innerchr10:129728257..130134062hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38405806
hg19405806
hg18405806
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv989n100
Supporting Variantsnssv3507469
Samples
Known GenesMKI67, PTPRE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043925
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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