A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362252



Internal ID22587921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:143270080..143335125hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3865046
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973177
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362252
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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