A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523076



Internal ID15450369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181087652..181151750hg38UCSC Ensembl
Innerchr5:180514652..180578750hg19UCSC Ensembl
Innerchr5:180447258..180511356hg18UCSC Ensembl
Innerchr5:180447258..180511356hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3864099
hg1964099
hg1864099
hg1764099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv365n21
Supporting Variantsnssv698766
Samples
Known GenesOR2V1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523076
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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