A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv715265



Internal ID16009221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:58449952..58470712hg38UCSC Ensembl
Innerchr1:58915624..58936384hg19UCSC Ensembl
Innerchr1:58688212..58708972hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3820761
hg1920761
hg1820761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546314
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv715265
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