A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568741



Internal ID20941812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134621267..134621822hg38UCSC Ensembl
chr5:133956957..133957512hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267325
Samples
Known GenesSAR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568741
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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