A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592846



Internal ID20965917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59402349..59413055hg38UCSC Ensembl
chr14:59869067..59879773hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3810707
hg1910707
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237140
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592846
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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