A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3515036



Internal ID18813317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:111591045..111608024hg38UCSC Ensembl
Innerchr10:113350803..113367782hg19UCSC Ensembl
Innerchr10:113340793..113357772hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3816980
hg1916980
hg1816980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052580
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3515036
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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