A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462673



Internal ID240597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:94709883..94882639hg38UCSC Ensembl
chr6:95419601..95592357hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38172757
hg19172757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv426n206
Supporting Variantsnssv16985112
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462673
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