A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520536



Internal ID18818817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86600459..86626553hg38UCSC Ensembl
Innerchr10:88360216..88386310hg19UCSC Ensembl
Innerchr10:88350196..88376290hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3826095
hg1926095
hg1826095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051614
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)nssv3520536
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