A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565638



Internal ID20938709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135623957..135625303hg38UCSC Ensembl
chr5:134959647..134960993hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg381347
hg191347
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267373
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565638
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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