A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550283



Internal ID15991006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:27855401..27878397hg38UCSC Ensembl
Innerchr10:28144330..28167326hg19UCSC Ensembl
Innerchr10:28184336..28207332hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3822997
hg1922997
hg1822997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv745547
Samples
Known GenesARMC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550283
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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