A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523614



Internal ID15450907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:58086358..58181691hg38UCSC Ensembl
Innerchr10:59846118..59941452hg19UCSC Ensembl
Innerchr10:59516124..59611458hg18UCSC Ensembl
Innerchr10:59516124..59611458hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3895334
hg1995335
hg1895335
hg1795335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699410
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523614
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer