A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5547589



Internal ID321422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144265496..144265496hg38UCSC Ensembl
chr6:144586632..144586632hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16970925
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5547589
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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