A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529297



Internal ID305325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28141688..28142247hg38UCSC Ensembl
chr17:26468714..26469273hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712332
Samples
Known GenesNLK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529297
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