A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970432



Internal ID22745367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13989132..13992444hg38UCSC Ensembl
chr10:14031132..14034444hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383313
hg193313
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359217
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970432
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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