A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv903789



Internal ID16197745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:11979560..11994220hg38UCSC Ensembl
Innerchr2:12119686..12134346hg19UCSC Ensembl
Innerchr2:12037137..12051797hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3814661
hg1914661
hg1814661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580999
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)nssv903789
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