A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550199



Internal ID16337608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20573498..20640390hg38UCSC Ensembl
Innerchr10:20862427..20929319hg19UCSC Ensembl
Innerchr10:20902433..20969325hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3866893
hg1966893
hg1866893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1001n54
Supporting Variantsnssv744700
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550199
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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