A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520732



Internal ID15448025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:22036638..22043580hg38UCSC Ensembl
Innerchr6:22036867..22043809hg19UCSC Ensembl
Innerchr6:22144846..22151788hg18UCSC Ensembl
Innerchr6:22144846..22151788hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386943
hg196943
hg186943
hg176943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv374n21
Supporting Variantsnssv697580
Samples
Known GenesCASC15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520732
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