A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546667



Internal ID16334076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:80460627..80577070hg38UCSC Ensembl
Innerchr1:80926312..81042755hg19UCSC Ensembl
Innerchr1:80698900..80815343hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38116444
hg19116444
hg18116444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv343n54
Supporting Variantsnssv718349
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546667
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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