A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527904



Internal ID15108511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51628463..51640140hg38UCSC Ensembl
Innerchr10:53388223..53399900hg19UCSC Ensembl
Innerchr10:53058229..53069906hg18UCSC Ensembl
Innerchr10:53058229..53069906hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3811678
hg1911678
hg1811678
hg1711678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704408
Samples
Known GenesPRKG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527904
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