A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990095



Internal ID60804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154953429..154955981hg38UCSC Ensembl
chr6:155274563..155277115hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg382553
hg192553
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459836
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990095
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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