A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663274



Internal ID15399926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:117448658..117450864hg38UCSC Ensembl
Innerchr10:119208169..119210375hg19UCSC Ensembl
Innerchr10:119198159..119200365hg18UCSC Ensembl
Innerchr10:119198159..119200365hg17UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg382207
hg192207
hg182207
hg172207
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516718
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663274
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