A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727147



Internal ID150813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44591021..44638540hg38UCSC Ensembl
chr21:46010902..46058457hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3847520
hg1947556
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147162
Supporting Variants
Samples
Known GenesKRTAP10-10, KRTAP10-6, KRTAP10-7, KRTAP10-8, KRTAP10-9, TSPEAR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727147
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.023111


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