A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469352



Internal ID247141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53196920..53202075hg38UCSC Ensembl
chr6:53061718..53066873hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg385156
hg195156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985952
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469352
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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