A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546679



Internal ID16334088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:81435320..81482245hg38UCSC Ensembl
Innerchr1:81901005..81947930hg19UCSC Ensembl
Innerchr1:81673593..81720518hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3846926
hg1946926
hg1846926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173043
Samples1788485381_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546679
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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