A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv930353



Internal ID15877623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:201644883..201666824hg38UCSC Ensembl
Innerchr2:202509606..202531547hg19UCSC Ensembl
Innerchr2:202217851..202239792hg18UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3821942
hg1921942
hg1821942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584162
Supporting Variants
Samples
Known GenesMPP4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv930353
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