A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589042



Internal ID20962113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73280074..73280846hg38UCSC Ensembl
chr14:73746782..73747554hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38773
hg19773
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238645
Samples
Known GenesNUMB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589042
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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