A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555244



Internal ID20928335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18614360..18615932hg38UCSC Ensembl
chr3:18655852..18657424hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg381573
hg191573
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261254
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555244
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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