A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16978083



Internal ID52794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6898164..6905282hg38UCSC Ensembl
chr6:6898397..6905515hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg387119
hg197119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463390
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16978083
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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