A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719596



Internal ID15666866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:93823114..93825696hg38UCSC Ensembl
Innerchr1:94288670..94291252hg19UCSC Ensembl
Innerchr1:94061258..94063840hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg382583
hg192583
hg182583
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546838
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)nssv719596
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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