A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528358



Internal ID15108965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148964410..149040285hg38UCSC Ensembl
Innerchr7:148661502..148737377hg19UCSC Ensembl
Innerchr7:148292435..148368310hg18UCSC Ensembl
Innerchr7:148099150..148175025hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3875876
hg1975876
hg1875876
hg1775876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704943
Samples
Known GenesPDIA4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528358
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