A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523927



Internal ID15104534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:39867354..39890024hg38UCSC Ensembl
Innerchr3:39908845..39931515hg19UCSC Ensembl
Innerchr3:39883849..39906519hg18UCSC Ensembl
Innerchr3:39883849..39906519hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3822671
hg1922671
hg1822671
hg1722671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699772
Samples
Known GenesMYRIP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523927
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