A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524428



Internal ID15451721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69292752..69296394hg38UCSC Ensembl
Innerchr10:71052508..71056150hg19UCSC Ensembl
Innerchr10:70722514..70726156hg18UCSC Ensembl
Innerchr10:70722514..70726156hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg383643
hg193643
hg183643
hg173643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700355
Samples
Known GenesHK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524428
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