A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584236



Internal ID16371645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:203319354..203326603hg38UCSC Ensembl
Innerchr2:204184077..204191326hg19UCSC Ensembl
Innerchr2:203892322..203899571hg18UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg387250
hg197250
hg187250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7262n54
Supporting Variantsnssv930594, nssv930595, nssv930593
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584236
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