A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563163



Internal ID20936234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153141820..153153581hg38UCSC Ensembl
chr4:154062972..154074733hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3811762
hg1911762
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263878
Samples
Known GenesTRIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563163
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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