A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477291



Internal ID21134844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:26368159..26369020hg38UCSC Ensembl
chr14:26837365..26838226hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38862
hg19862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016893
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477291
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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