A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523982



Internal ID15451275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:22036638..22044787hg38UCSC Ensembl
Innerchr6:22036867..22045016hg19UCSC Ensembl
Innerchr6:22144846..22152995hg18UCSC Ensembl
Innerchr6:22144846..22152995hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg388150
hg198150
hg188150
hg178150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv374n21
Supporting Variantsnssv699838
Samples
Known GenesCASC15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523982
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