A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984700



Internal ID57188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42878277..42878701hg38UCSC Ensembl
chr6:42846015..42846439hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557526
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984700
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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