A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403271



Internal ID22461141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47328588..47329627hg38UCSC Ensembl
chr20:45957332..45958371hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg381040
hg191040
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971784
Supporting Variants
Samples
Known GenesZMYND8
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403271
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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