A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4020631



Internal ID22082262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10527389..10531886hg38UCSC Ensembl
Outerchr5:10525504..10532403hg38UCSC Ensembl
Innerchr5:10527501..10531998hg19UCSC Ensembl
Outerchr5:10525616..10532515hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156312
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4020631
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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