A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516911



Internal ID293353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81690487..81690553hg38UCSC Ensembl
chr17:79657517..79657583hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17715605
Samples
Known GenesHGS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516911
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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