A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670243



Internal ID21618550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:254720..365488hg38UCSC Ensembl
chr5:254835..365603hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38110769
hg19110769
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133123
Samples
Known GenesAHRR, LOC102467073, PDCD6, SDHA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670243
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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