A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571438



Internal ID20944509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:59162674..59163124hg38UCSC Ensembl
chr5:58458501..58458951hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268923
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571438
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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