A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583498



Internal ID16024221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:161155624..161268783hg38UCSC Ensembl
Innerchr2:162012135..162125294hg19UCSC Ensembl
Innerchr2:161720381..161833540hg18UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38113160
hg19113160
hg18113160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7140n54
Supporting Variantsnssv923514
Samples
Known GenesTANK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583498
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