A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369421



Internal ID22595090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101425613..102066292hg38UCSC Ensembl
chr1:101891169..102531848hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38640680
hg19640680
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971241
Supporting Variants
Samples
Known GenesDNAJA1P5, OLFM3
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369421
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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