A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563321



Internal ID20936392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112399766..112400568hg38UCSC Ensembl
chr3:112118613..112119415hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38803
hg19803
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259202
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563321
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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