A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990716



Internal ID61222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169751830..169751844hg38UCSC Ensembl
chr6:170151926..170151940hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552611
Supporting Variants
Samples
Known GenesERMARD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990716
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002342


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