A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359893



Internal ID22585562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23505012..23505101hg38UCSC Ensembl
chr1:23831504..23831593hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972179
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359893
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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