A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515253



Internal ID291736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:20993552..20998383hg38UCSC Ensembl
chr17:20896865..20901696hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg384832
hg194832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712133
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515253
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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