A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040566



Internal ID19129785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:118414274..118445777hg38UCSC Ensembl
Innerchr10:120173786..120205289hg19UCSC Ensembl
Innerchr10:120163776..120195279hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3831504
hg1931504
hg1831504
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507770
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)nsv1040566
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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