A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535333



Internal ID310982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159761887..159761917hg38UCSC Ensembl
chr6:160182919..160182949hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989209
Samples
Known GenesLOC100129518
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535333
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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