A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580696



Internal ID20953767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:50327212..50327463hg38UCSC Ensembl
chr14:50793930..50794181hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580696
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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