A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977931



Internal ID52691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:196713..448068hg38UCSC Ensembl
chr6:196713..448068hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38251356
hg19251356
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562360
Supporting Variants
Samples
Known GenesDUSP22, IRF4
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977931
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001405


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