A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583862



Internal ID20956933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69227700..69228195hg38UCSC Ensembl
chr14:69694417..69694912hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237942
Samples
Known GenesEXD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583862
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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