A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478818



Internal ID21136371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76849668..76850678hg38UCSC Ensembl
chr14:77316011..77317021hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381011
hg191011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021204
Samples
Known GenesC14orf166B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478818
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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