A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580772



Internal ID16368181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:3344449..3378347hg38UCSC Ensembl
Innerchr2:3348220..3382118hg19UCSC Ensembl
Innerchr2:3327227..3361125hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3833899
hg1933899
hg1833899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv902731
Samples
Known GenesTSSC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580772
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