A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv903223



Internal ID16197179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4165788..4189215hg38UCSC Ensembl
Innerchr2:4213378..4236805hg19UCSC Ensembl
Innerchr2:4191253..4214680hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3823428
hg1923428
hg1823428
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580843
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)nssv903223
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