A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535702



Internal ID311300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:30335551..30335590hg38UCSC Ensembl
chr6:30303328..30303367hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16983423
Samples
Known GenesTRIM39, TRIM39-RPP21
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535702
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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