A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528172



Internal ID15108779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26430753..26463432hg38UCSC Ensembl
Innerchr6:26430981..26463660hg19UCSC Ensembl
Innerchr6:26538960..26571639hg18UCSC Ensembl
Innerchr6:26538960..26571639hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3832680
hg1932680
hg1832680
hg1732680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704721
Samples
Known GenesBTN2A1, BTN3A3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528172
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