A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702059



Internal ID15092025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89180930..89184902hg38UCSC Ensembl
Innerchr10:90940687..90944659hg19UCSC Ensembl
Innerchr10:90930667..90934639hg18UCSC Ensembl
Innerchr10:90930667..90934639hg17UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg383973
hg193973
hg183973
hg173973
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517170
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702059
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