A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591111



Internal ID20964182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73452082..73453146hg38UCSC Ensembl
chr14:73918789..73919853hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381065
hg191065
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2196n223
Supporting Variantsnssv18238673
Samples
Known GenesNUMB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591111
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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