A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581125



Internal ID20954196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85870427..85889304hg38UCSC Ensembl
chr14:86336771..86355648hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3818878
hg1918878
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237563
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581125
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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