A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485293



Internal ID21142846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74911162..74913729hg38UCSC Ensembl
chr14:75377865..75380432hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382568
hg192568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021113
Samples
Known GenesRPS6KL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485293
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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