A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971751



Internal ID22746686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48640771..48658698hg38UCSC Ensembl
chr10:49848816..49866743hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3817928
hg1917928
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369388
Samples
Known GenesARHGAP22
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971751
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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