A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413151



Internal ID22471021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43154861..43156084hg38UCSC Ensembl
chr5:43154963..43156186hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg381224
hg191224
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978158
Supporting Variants
Samples
Known GenesZNF131
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413151
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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