A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590450



Internal ID20963521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74691138..74692607hg38UCSC Ensembl
chr14:75157841..75159310hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381470
hg191470
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2207n223
Supporting Variantsnssv18237272
Samples
Known GenesAREL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590450
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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