A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550815



Internal ID15991538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48566588..48586436hg38UCSC Ensembl
Innerchr10:49774633..49794481hg19UCSC Ensembl
Innerchr10:49444639..49464487hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3819849
hg1919849
hg1819849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv747654
Samples
Known GenesARHGAP22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550815
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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