A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546682



Internal ID16334091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:82525950..82579128hg38UCSC Ensembl
Innerchr1:82991633..83044811hg19UCSC Ensembl
Innerchr1:82764221..82817399hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3853179
hg1953179
hg1853179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv718374
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546682
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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