A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478038



Internal ID21135591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45485820..45583340hg38UCSC Ensembl
chr14:45955023..46052543hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3897521
hg1997521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018903
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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