A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662458



Internal ID15052424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2650464..3035272hg38UCSC Ensembl
Innerchr10:2692656..3077464hg19UCSC Ensembl
Innerchr10:2682656..3067464hg18UCSC Ensembl
Innerchr10:2682656..3067464hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38384809
hg19384809
hg18384809
hg17384809
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517630
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662458
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