A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395713



Internal ID22453583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34327019..34329014hg38UCSC Ensembl
chr20:32914825..32916820hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381996
hg191996
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978243
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395713
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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