A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980199



Internal ID54172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27509842..27509893hg38UCSC Ensembl
chr6:27477621..27477672hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560335
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980199
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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