A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594970



Internal ID20968041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73855644..73855921hg38UCSC Ensembl
chr14:74322347..74322624hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2201n223
Supporting Variantsnssv18238694
Samples
Known GenesPTGR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594970
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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