A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485364



Internal ID21142917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75055983..75068201hg38UCSC Ensembl
chr14:75522686..75534904hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3812219
hg1912219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021119
Samples
Known GenesACYP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485364
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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