A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550129



Internal ID16337538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19128252..19545866hg38UCSC Ensembl
Innerchr10:19417181..19834795hg19UCSC Ensembl
Innerchr10:19457187..19874801hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38417615
hg19417615
hg18417615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744284
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550129
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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