A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563191



Internal ID20936262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114238169..114241171hg38UCSC Ensembl
chr5:113573866..113576868hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg383003
hg193003
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266594
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563191
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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