A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155880



Internal ID22086385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:163786978..163788616hg38UCSC Ensembl
Outerchr2:163780342..163790132hg38UCSC Ensembl
Innerchr2:164643488..164645126hg19UCSC Ensembl
Outerchr2:164636852..164646642hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg389791
hg199791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv175n97
Supporting Variantsnssv4014638, nssv4014640, nssv4014641, nssv4015304, nssv4014636, nssv4014637, nssv4014642, nssv4014639, nssv4015303
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155880
Frequency
Sample Size131
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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