A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527268



Internal ID15454561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176203096..176247562hg38UCSC Ensembl
Innerchr3:175920884..175965350hg19UCSC Ensembl
Innerchr3:177403578..177448044hg18UCSC Ensembl
Innerchr3:177403586..177448052hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3844467
hg1944467
hg1844467
hg1744467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703676
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527268
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