A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489922



Internal ID21147475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45904830..46013712hg38UCSC Ensembl
chr14:46374033..46482915hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38108883
hg19108883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018964
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489922
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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