A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369481



Internal ID22595150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:181092770..181093503hg38UCSC Ensembl
chr1:181061906..181062639hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978627
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369481
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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