A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046158



Internal ID19135377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8658738..8687776hg38UCSC Ensembl
Innerchr10:8700701..8729739hg19UCSC Ensembl
Innerchr10:8740707..8769745hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3829039
hg1929039
hg1829039
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv670n100
Supporting Variantsnssv3491250
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046158
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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