A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475700



Internal ID21133253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28794322..28861069hg38UCSC Ensembl
chr14:29263528..29330275hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3866748
hg1966748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017221
Samples
Known GenesC14orf23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475700
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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