A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571642



Internal ID20944713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113707130..113707549hg38UCSC Ensembl
chr3:113425977..113426396hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38420
hg19420
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259245
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571642
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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