A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978662



Internal ID22753597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:53976868..54005627hg38UCSC Ensembl
chr17:52054229..52082988hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3828760
hg1928760
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377204
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978662
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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