A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587811



Internal ID20960882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23504293..23504564hg38UCSC Ensembl
chr14:23973502..23973773hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235503
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587811
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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