A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156332



Internal ID22084808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:41231396..41241291hg38UCSC Ensembl
Outerchr5:41226663..41244575hg38UCSC Ensembl
Innerchr5:41231498..41241393hg19UCSC Ensembl
Outerchr5:41226765..41244677hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3817913
hg1917913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020805, nssv4020804
Samples
Known GenesC6
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156332
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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