A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516625



Internal ID293076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35193918..35229678hg38UCSC Ensembl
chr17:33520937..33556697hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3835761
hg1935761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712796
Samples
Known GenesSLC35G3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516625
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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