A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550040



Internal ID16337449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:18076451..18110590hg38UCSC Ensembl
Innerchr10:18365380..18399519hg19UCSC Ensembl
Innerchr10:18405386..18439525hg18UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3834140
hg1934140
hg1834140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744147
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550040
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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