A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550039



Internal ID16337448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:18074995..18136590hg38UCSC Ensembl
Innerchr10:18363924..18425519hg19UCSC Ensembl
Innerchr10:18403930..18465525hg18UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3861596
hg1961596
hg1861596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744146
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550039
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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