A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416478



Internal ID22474348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87937547..87949082hg38UCSC Ensembl
chr4:88858699..88870234hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3811536
hg1911536
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979114
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416478
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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