A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564533



Internal ID20937604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87396447..87397220hg38UCSC Ensembl
chr5:86692264..86693037hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38774
hg19774
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269699
Samples
Known GenesCCNH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564533
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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