A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977977



Internal ID52721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2998054..3056986hg38UCSC Ensembl
chr6:2998288..3057220hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3858933
hg1958933
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554622
Supporting Variants
Samples
Known GenesHTATSF1P2, NQO2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977977
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.009994


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