A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550153



Internal ID16337562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20494784..20525654hg38UCSC Ensembl
Innerchr10:20783713..20814583hg19UCSC Ensembl
Innerchr10:20823719..20854589hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3830871
hg1930871
hg1830871
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv990n54
Supporting Variantsnssv744328
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550153
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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