A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967562



Internal ID22742497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37415697..37416258hg38UCSC Ensembl
chr17:35775781..35776343hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38562
hg19563
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377009
Samples
Known GenesTADA2A
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967562
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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