A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584115



Internal ID20957186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:29549631..29550690hg38UCSC Ensembl
chr14:30018837..30019896hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg381060
hg191060
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236705
Samples
Known GenesMIR548AI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584115
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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