A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546668



Internal ID16334077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:80498805..80586373hg38UCSC Ensembl
Innerchr1:80964490..81052058hg19UCSC Ensembl
Innerchr1:80737078..80824646hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3887569
hg1987569
hg1887569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv718351, nssv718350
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546668
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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