A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5518865



Internal ID295229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81614190..81616602hg38UCSC Ensembl
chr17:79581216..79583628hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382413
hg192413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17715595
Samples
Known GenesNPLOC4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5518865
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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