A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575975



Internal ID20949046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:72822195..72824562hg38UCSC Ensembl
chr14:73288903..73291270hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg382368
hg192368
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238625
Samples
Known GenesDPF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575975
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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