A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402823



Internal ID22460693
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 StatusS
Merged Variantsnsv5978189
Supporting Variants
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)nssv17402823
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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