A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519517



Internal ID295865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51680528..51680585hg38UCSC Ensembl
chr17:49757888..49757945hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17713618
Samples
Known GenesCA10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519517
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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