A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977796



Internal ID22752731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22029244..22112233hg38UCSC Ensembl
chr1:22355737..22438726hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3882990
hg1982990
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363825
Samples
Known GenesCDC42, LINC00339
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977796
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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