A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433366



Internal ID212086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64889980..64899490hg38UCSC Ensembl
chr17:62886098..62895608hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg389511
hg199511
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714100
Samples
Known GenesLRRC37A3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433366
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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