A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586925



Internal ID20959996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:53124130..53125932hg38UCSC Ensembl
chr14:53590848..53592650hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg381803
hg191803
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237753
Samples
Known GenesDDHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586925
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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