A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582179



Internal ID20955250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35388822..35390118hg38UCSC Ensembl
chr14:35858028..35859324hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg381297
hg191297
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218913
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582179
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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