A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594497



Internal ID20967568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30580397..30581387hg38UCSC Ensembl
chr14:31049603..31050593hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38991
hg19991
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231958
Samples
Known GenesG2E3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594497
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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