A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578271



Internal ID20951342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85633573..85633687hg38UCSC Ensembl
chr14:86099917..86100031hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237561
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578271
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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