A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579131



Internal ID20952202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23338965..23340102hg38UCSC Ensembl
chr14:23808174..23809311hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381138
hg191138
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2063n223
Supporting Variantsnssv18222069
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579131
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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