A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16969180



Internal ID46776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135181137..135181158hg38UCSC Ensembl
chr6:135502275..135502296hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535770
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16969180
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001561


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