A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582105



Internal ID20955176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35884848..35885415hg38UCSC Ensembl
chr14:36354054..36354621hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38568
hg19568
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2099n223
Supporting Variantsnssv18220993
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582105
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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