A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527037



Internal ID15454330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29648045..29656335hg38UCSC Ensembl
Innerchr6:29615822..29624112hg19UCSC Ensembl
Innerchr6:29723801..29732091hg18UCSC Ensembl
Innerchr6:29723801..29732091hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg388291
hg198291
hg188291
hg178291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703413
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527037
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