A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16982481



Internal ID55679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29665311..29665779hg38UCSC Ensembl
chr6:29633088..29633556hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562335
Supporting Variants
Samples
Known GenesMOG
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16982481
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.066812


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