A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373477



Internal ID22599146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66994598..67008200hg38UCSC Ensembl
chr1:67460281..67473883hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3813603
hg1913603
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977657
Supporting Variants
Samples
Known GenesSLC35D1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373477
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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