A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978189



Internal ID22753124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44550659..44628117hg38UCSC Ensembl
chr21:45970542..46048034hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3877459
hg1977493
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402823
Samples
Known GenesKRTAP10-2, KRTAP10-3, KRTAP10-4, KRTAP10-5, KRTAP10-6, KRTAP10-7, KRTAP10-8, KRTAP10-9, TSPEAR
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978189
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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