A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv924942



Internal ID16218898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:163256297..163288670hg38UCSC Ensembl
Innerchr2:164112807..164145180hg19UCSC Ensembl
Innerchr2:163821053..163853426hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3832374
hg1932374
hg1832374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583526
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)nssv924942
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