A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581687



Internal ID16369096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:44240247..44241062hg38UCSC Ensembl
Innerchr2:44467386..44468201hg19UCSC Ensembl
Innerchr2:44320890..44321705hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38816
hg19816
hg18816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6836n54
Supporting Variantsnssv907980, nssv907982, nssv907981
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581687
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer