A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986888



Internal ID58703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92442710..92468129hg38UCSC Ensembl
chr6:93152428..93177847hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3825420
hg1925420
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562422
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986888
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


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