A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567085



Internal ID20940156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72864910..72865354hg38UCSC Ensembl
chr5:72160737..72161181hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267058
Samples
Known GenesTNPO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567085
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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