A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546666



Internal ID16334075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:80443732..80586373hg38UCSC Ensembl
Innerchr1:80909417..81052058hg19UCSC Ensembl
Innerchr1:80682005..80824646hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38142642
hg19142642
hg18142642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv343n54
Supporting Variantsnssv718348
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546666
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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