A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977976



Internal ID52720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2997997..3056987hg38UCSC Ensembl
chr6:2998231..3057221hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3858991
hg1958991
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554691
Supporting Variants
Samples
Known GenesHTATSF1P2, NQO2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977976
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.010615


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