A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563804



Internal ID20936875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155855485..155855830hg38UCSC Ensembl
chr3:155573274..155573619hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260419
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563804
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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