A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695692



Internal ID15432344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75982171..75991601hg38UCSC Ensembl
Innerchr15:76274512..76283942hg19UCSC Ensembl
Innerchr15:74061567..74070997hg18UCSC Ensembl
Innerchr15:74061567..74070997hg17UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg389431
hg199431
hg189431
hg179431
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518261
Supporting Variants
Samples
Known GenesNRG4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695692
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