A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518399



Internal ID15445692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:53721717..53727002hg38UCSC Ensembl
Innerchr7:53789410..53794695hg19UCSC Ensembl
Innerchr7:53756904..53762189hg18UCSC Ensembl
Innerchr7:53563619..53568904hg17UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg385286
hg195286
hg185286
hg175286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695829
Samples
Known GenesFLJ45974
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518399
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