A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719610



Internal ID15666880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:93824138..93825696hg38UCSC Ensembl
Innerchr1:94289694..94291252hg19UCSC Ensembl
Innerchr1:94062282..94063840hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg381559
hg191559
hg181559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546847
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)nssv719610
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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