A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5472051



Internal ID249771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29690836..29690930hg38UCSC Ensembl
chr6:29658613..29658707hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982485
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5472051
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