A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567291



Internal ID20940362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149477281..149478462hg38UCSC Ensembl
chr5:148856844..148858025hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381182
hg191182
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268674
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567291
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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