A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5399901



Internal ID179287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157794783..157794783hg38UCSC Ensembl
chr6:158215815..158215815hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16990102
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5399901
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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