A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591347



Internal ID20964418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:50628847..50629583hg38UCSC Ensembl
chr14:51095565..51096301hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236268
Samples
Known GenesATL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591347
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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