A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527527



Internal ID303625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2525038..2532908hg38UCSC Ensembl
chr17:2428332..2436202hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg387871
hg197871
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709977
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527527
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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