A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156048



Internal ID22086553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:172593922..172600018hg38UCSC Ensembl
Outerchr3:172591663..172601655hg38UCSC Ensembl
Innerchr3:172311712..172317808hg19UCSC Ensembl
Outerchr3:172309453..172319445hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg389993
hg199993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv206n97
Supporting Variantsnssv4016102
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156048
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