A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588887



Internal ID20961958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61363731..61384389hg38UCSC Ensembl
chr14:61830449..61851107hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3820659
hg1920659
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237176
Samples
Known GenesPRKCH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588887
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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