A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446484



Internal ID22504354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25064145..25077276hg38UCSC Ensembl
chr6:25064373..25077504hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3813132
hg1913132
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971832
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446484
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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