A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550128



Internal ID16337537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19111916..19690505hg38UCSC Ensembl
Innerchr10:19400845..19979434hg19UCSC Ensembl
Innerchr10:19440851..20019440hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38578590
hg19578590
hg18578590
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174143
SamplesHGDP01287
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550128
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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