A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517963



Internal ID15445256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80245151..80257955hg38UCSC Ensembl
Innerchr7:79874467..79887271hg19UCSC Ensembl
Innerchr7:79712403..79725207hg18UCSC Ensembl
Innerchr7:79519118..79531922hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3812805
hg1912805
hg1812805
hg1712805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694186
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517963
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