A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571582



Internal ID20944653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133093586..133094040hg38UCSC Ensembl
chr5:132429278..132429732hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5938n223
Supporting Variantsnssv18266686
Samples
Known GenesHSPA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571582
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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