A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990719



Internal ID61224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169771709..169771837hg38UCSC Ensembl
chr6:170171805..170171933hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5456133
Supporting Variants
Samples
Known GenesERMARD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990719
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001561


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