A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463256



Internal ID241164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83270882..83270938hg38UCSC Ensembl
chr6:83980601..83980657hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16983970
Samples
Known GenesME1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463256
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