A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581708



Internal ID20954779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:26436050..26436444hg38UCSC Ensembl
chr14:26905256..26905650hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232530
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581708
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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