A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583670



Internal ID20956741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102324646..102325553hg38UCSC Ensembl
chr14:102790983..102791890hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38908
hg19908
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229660
Samples
Known GenesZNF839
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583670
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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