A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989442



Internal ID60388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155325949..155326000hg38UCSC Ensembl
chr6:155647083..155647134hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg385998
hg195998
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556840
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989442
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003911


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