A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587927



Internal ID20960998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92096527..92096845hg38UCSC Ensembl
chr14:92562871..92563189hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237712
Samples
Known GenesATXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587927
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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