A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564785



Internal ID20937856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2028161..2050300hg38UCSC Ensembl
chr5:2028275..2050414hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3822140
hg1922140
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266298
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564785
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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