A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv908717



Internal ID16202673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:52345029..52429456hg38UCSC Ensembl
Innerchr2:52572167..52656594hg19UCSC Ensembl
Innerchr2:52425671..52510098hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3884428
hg1984428
hg1884428
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581928
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)nssv908717
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