A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495000



Internal ID21152553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22990593..22992961hg38UCSC Ensembl
chr14:23459802..23462170hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg382369
hg192369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016720
Samples
Known GenesC14orf93
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495000
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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