A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548493



Internal ID16335902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:189080886..189341528hg38UCSC Ensembl
Innerchr1:189050017..189310658hg19UCSC Ensembl
Innerchr1:187316640..187577281hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38260643
hg19260642
hg18260642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv732527
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548493
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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