A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719584



Internal ID15666854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:93822968..93828634hg38UCSC Ensembl
Innerchr1:94288524..94294190hg19UCSC Ensembl
Innerchr1:94061112..94066778hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg385667
hg195667
hg185667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546831
Supporting Variants
Samples
Known GenesBCAR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv719584
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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