A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548483



Internal ID16335892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:188833411..189703098hg38UCSC Ensembl
Innerchr1:188802542..189672228hg19UCSC Ensembl
Innerchr1:187069165..187938851hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38869688
hg19869687
hg18869687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv732519
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548483
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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