A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588933



Internal ID20962004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31029696..31030057hg38UCSC Ensembl
chr14:31498902..31499263hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232547
Samples
Known GenesAP4S1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588933
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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