A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406084



Internal ID21063637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151932015..151932543hg38UCSC Ensembl
chr5:151311576..151312104hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126949
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406084
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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