A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578095



Internal ID20951166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21715074..21715743hg38UCSC Ensembl
chr14:22183297..22183967hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38670
hg19671
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222205
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578095
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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