A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560926



Internal ID20933997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168836138..168836268hg38UCSC Ensembl
chr5:168263143..168263273hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267606
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560926
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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