A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491563



Internal ID21149116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:53616755..53628377hg38UCSC Ensembl
chr14:54083473..54095095hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3811623
hg1911623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019348
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491563
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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