A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579398



Internal ID20952469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63720684..63721154hg38UCSC Ensembl
chr14:64187402..64187872hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237336
Samples
Known GenesSGPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579398
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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