A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv920281



Internal ID16214237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:145380509..145466590hg38UCSC Ensembl
Innerchr2:146138077..146224158hg19UCSC Ensembl
Innerchr2:145854547..145940628hg18UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3886082
hg1986082
hg1886082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583249
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)nssv920281
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