A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595505



Internal ID20968576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21470262..21470849hg38UCSC Ensembl
chr14:21938421..21939008hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220311
Samples
Known GenesRAB2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595505
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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