A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719339



Internal ID15666609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:93822968..93825527hg38UCSC Ensembl
Innerchr1:94288524..94291083hg19UCSC Ensembl
Innerchr1:94061112..94063671hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg382560
hg192560
hg182560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546828
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)nssv719339
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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