A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591600



Internal ID20964671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23338954..23340052hg38UCSC Ensembl
chr14:23808163..23809261hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381099
hg191099
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2063n223
Supporting Variantsnssv18219780
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591600
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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