A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569739



Internal ID20942810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:145437396..145439587hg38UCSC Ensembl
chr5:144816959..144819150hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382192
hg192192
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268001
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569739
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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