A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719589



Internal ID15666859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:93823114..93824497hg38UCSC Ensembl
Innerchr1:94288670..94290053hg19UCSC Ensembl
Innerchr1:94061258..94062641hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg381384
hg191384
hg181384
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546833
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)nssv719589
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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