A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580491



Internal ID16367900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:1042045..1220708hg38UCSC Ensembl
Innerchr2:1037731..1216394hg19UCSC Ensembl
Innerchr2:1027731..1206395hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38178664
hg19178664
hg18178665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv902166
Samples
Known GenesSNTG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580491
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