A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048143



Internal ID19137362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:58080408..58132085hg38UCSC Ensembl
Innerchr10:59840168..59891846hg19UCSC Ensembl
Innerchr10:59510174..59561852hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3851678
hg1951679
hg1851679
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv876n100
Supporting Variantsnssv3521006, nssv3505680
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)nsv1048143
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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