A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585846



Internal ID20958917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23339011..23340080hg38UCSC Ensembl
chr14:23808220..23809289hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381070
hg191070
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2063n223
Supporting Variantsnssv18225118
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585846
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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