A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv907888



Internal ID15855158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:43225479..43227253hg38UCSC Ensembl
Innerchr2:43452618..43454392hg19UCSC Ensembl
Innerchr2:43306122..43307896hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381775
hg191775
hg181775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581651
Supporting Variants
Samples
Known GenesLINC01126, ZFP36L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv907888
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