A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011067



Internal ID22072698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:45444898..45456554hg38UCSC Ensembl
Outerchr15:45442613..45464885hg38UCSC Ensembl
Innerchr15:45737096..45748752hg19UCSC Ensembl
Outerchr15:45734811..45757083hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3822273
hg1922273
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155173
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011067
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