A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5544438



Internal ID318583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48638498..48638498hg38UCSC Ensembl
chr17:46715860..46715860hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17713566
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5544438
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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