A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587535



Internal ID20960606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102003280..102003905hg38UCSC Ensembl
chr14:102469617..102470242hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223423
Samples
Known GenesDYNC1H1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587535
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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