A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571577



Internal ID20944648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:19639226..21099504hg38UCSC Ensembl
chr5:19639335..21099613hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg381460279
hg191460279
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268291
Samples
Known GenesCDH18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571577
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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