A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976068



Internal ID22751003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107321755..107323029hg38UCSC Ensembl
chr13:107974103..107975377hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg381275
hg191275
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351769
Samples
Known GenesFAM155A
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976068
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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