A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528095



Internal ID15455388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110632371..110662639hg38UCSC Ensembl
Innerchr7:110272427..110302695hg19UCSC Ensembl
Innerchr7:110059663..110089931hg18UCSC Ensembl
Innerchr7:109866378..109896646hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3830269
hg1930269
hg1830269
hg1730269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv426n21
Supporting Variantsnssv704633
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528095
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