A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558020



Internal ID20931091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:59613768..59627849hg38UCSC Ensembl
chr5:58909594..58923675hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3814082
hg1914082
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268926
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558020
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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