A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576831



Internal ID20949902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24386037..24386463hg38UCSC Ensembl
chr14:24855243..24855669hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2076n223
Supporting Variantsnssv18235612
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576831
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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