A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555841



Internal ID20928912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43455191..43455704hg38UCSC Ensembl
chr5:43455293..43455806hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268399
Samples
Known GenesC5orf28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555841
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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