A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586889



Internal ID20959960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49628943..49630183hg38UCSC Ensembl
chr14:50095661..50096901hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg381241
hg191241
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225617
Samples
Known GenesDNAAF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586889
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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