A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517330



Internal ID293756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75186423..75204136hg38UCSC Ensembl
chr17:73182518..73200231hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3817714
hg1917714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714610
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517330
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