A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5531532



Internal ID307489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78176213..78176290hg38UCSC Ensembl
chr17:76172294..76172371hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714836
Samples
Known GenesTK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5531532
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