A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521102



Internal ID15448395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1891874..1942566hg38UCSC Ensembl
Innerchr10:1934068..1984760hg19UCSC Ensembl
Innerchr10:1924068..1974760hg18UCSC Ensembl
Innerchr10:1924068..1974760hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3850693
hg1950693
hg1850693
hg1750693
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697788
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521102
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