A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516785



Internal ID293233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19426917..19433602hg38UCSC Ensembl
chr17:19330230..19336915hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg386686
hg196686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711999
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516785
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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