A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3504346



Internal ID18802627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:111303520..111319032hg38UCSC Ensembl
Innerchr10:113063278..113078790hg19UCSC Ensembl
Innerchr10:113053268..113068780hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3815513
hg1915513
hg1815513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037843
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)nssv3504346
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