A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571788



Internal ID20944859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138022121..138022847hg38UCSC Ensembl
chr5:137357810..137358536hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266792
Samples
Known GenesFAM13B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571788
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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