A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528653



Internal ID15455946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148765085..148771525hg38UCSC Ensembl
Innerchr7:148462177..148468617hg19UCSC Ensembl
Innerchr7:148093110..148099550hg18UCSC Ensembl
Innerchr7:147899825..147906265hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg386441
hg196441
hg186441
hg176441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705287
Samples
Known GenesCUL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528653
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