A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593076



Internal ID20966147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19749605..19749984hg38UCSC Ensembl
chr14:20217764..20218143hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223251
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593076
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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