A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv722259



Internal ID16016215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:110581114..110618388hg38UCSC Ensembl
Innerchr1:111123736..111161010hg19UCSC Ensembl
Innerchr1:110925259..110962533hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3837275
hg1937275
hg1837275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547499
Supporting Variants
Samples
Known GenesKCNA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv722259
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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