A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747652



Internal ID15694922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48461099..48527518hg38UCSC Ensembl
Innerchr10:49669142..49735563hg19UCSC Ensembl
Innerchr10:49339148..49405569hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3866420
hg1966422
hg1866422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550813
Supporting Variants
Samples
Known GenesARHGAP22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv747652
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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