A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493404



Internal ID21150957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:56340964..56341833hg38UCSC Ensembl
chr14:56807682..56808551hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38870
hg19870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019557
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493404
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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