A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594579



Internal ID20967650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35873996..35874509hg38UCSC Ensembl
chr14:36343202..36343715hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233470
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594579
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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