A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535444



Internal ID311081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126222911..126222913hg38UCSC Ensembl
chr6:126544057..126544059hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16969646
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535444
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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