A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546826



Internal ID15987549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:93822968..93825150hg38UCSC Ensembl
Innerchr1:94288524..94290706hg19UCSC Ensembl
Innerchr1:94061112..94063294hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg382183
hg192183
hg182183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv369n54
Supporting Variantsnssv719332, nssv719333, nssv719334, nssv719335
Samples
Known GenesBCAR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546826
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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