A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5531960



Internal ID307895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75164259..75167129hg38UCSC Ensembl
chr17:73160354..73163224hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg382871
hg192871
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714605
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5531960
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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