A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv711293



Internal ID15658563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:22018600..22063579hg38UCSC Ensembl
Innerchr1:22345093..22390072hg19UCSC Ensembl
Innerchr1:22217680..22262659hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3844980
hg1944980
hg1844980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545745
Supporting Variants
Samples
Known GenesCDC42, LINC00339
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv711293
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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