A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580870



Internal ID20953941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20926774..20959292hg38UCSC Ensembl
chr14:21394933..21427451hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3832519
hg1932519
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236005
Samples
Known GenesRNASE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580870
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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