A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485407



Internal ID21142960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59861145..59934943hg38UCSC Ensembl
chr14:60327863..60401661hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3873799
hg1973799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020449
Samples
Known GenesLRRC9, RTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485407
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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