A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380560



Internal ID22438430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32205004..32205790hg38UCSC Ensembl
chr13:32779141..32779927hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38787
hg19787
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975691
Supporting Variants
Samples
Known GenesFRY
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380560
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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