A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5547691



Internal ID321513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98387823..98387823hg38UCSC Ensembl
chr6:98835699..98835699hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5547691
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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