A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990008



Internal ID60749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151156439..151160264hg38UCSC Ensembl
chr6:151477574..151481399hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg383826
hg193826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458618
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990008
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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