A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528267



Internal ID15455560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:93218118..93286053hg38UCSC Ensembl
Innerchr7:92847431..92915365hg19UCSC Ensembl
Innerchr7:92685367..92753301hg18UCSC Ensembl
Innerchr7:92492082..92560016hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3867936
hg1967935
hg1867935
hg1767935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704835
Samples
Known GenesCCDC132, HEPACAM2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528267
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