A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16988954



Internal ID60061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148969163..148973074hg38UCSC Ensembl
chr6:149290299..149294210hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg383912
hg193912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468255
Supporting Variants
Samples
Known GenesUST
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16988954
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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