A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565514



Internal ID20938585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122750062..122752275hg38UCSC Ensembl
chr5:122085757..122087970hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg382214
hg192214
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266211
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565514
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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