A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546669



Internal ID16334078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:80747663..80814625hg38UCSC Ensembl
Innerchr1:81213348..81280310hg19UCSC Ensembl
Innerchr1:80985936..81052898hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3866963
hg1966963
hg1866963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv718352, nssv718353, nssv718354
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546669
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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