A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv732833



Internal ID16026789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:194316563..194355337hg38UCSC Ensembl
Innerchr1:194285693..194324467hg19UCSC Ensembl
Innerchr1:192552316..192591090hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3838775
hg1938775
hg1838775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548667
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv732833
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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