A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719329



Internal ID15666599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:93822968..93824915hg38UCSC Ensembl
Innerchr1:94288524..94290471hg19UCSC Ensembl
Innerchr1:94061112..94063059hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg381948
hg191948
hg181948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546825
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)nssv719329
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer