A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979622



Internal ID22754557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:71089972..71167591hg38UCSC Ensembl
chr4:71955689..72033308hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3877620
hg1977620
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426300
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979622
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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