A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020503



Internal ID19109722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:101659803..101947452hg38UCSC Ensembl
Innerchr5:100995507..101283156hg19UCSC Ensembl
Innerchr5:101023406..101311055hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38287650
hg19287650
hg18287650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5742n100
Supporting Variantsnssv3645829
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)nsv1020503
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