A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370533



Internal ID22596202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78315967..78316341hg38UCSC Ensembl
chr17:76312048..76312422hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975010
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370533
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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