A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528477



Internal ID304533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21047681..21056987hg38UCSC Ensembl
chr17:20950994..20960300hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg389307
hg199307
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712137, nssv17712136
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528477
Frequency
Sample Size3202
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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