A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984613



Internal ID57124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74069808..74069859hg38UCSC Ensembl
chr6:74779524..74779575hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38806
hg19806
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555888
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984613
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000469


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