A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5552116



Internal ID325519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148277734..148277771hg38UCSC Ensembl
chr6:148598870..148598907hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989285
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5552116
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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