A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587841



Internal ID20960912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77382751..77383990hg38UCSC Ensembl
chr14:77849094..77850333hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237522
Samples
Known GenesSAMD15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587841
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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