A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983124



Internal ID56129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41073936..41073936hg38UCSC Ensembl
chr6:41041675..41041675hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381
hg191
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563520
Supporting Variants
Samples
Known GenesNFYA
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983124
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.004839


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