A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481899



Internal ID21139452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:48221733..48240589hg38UCSC Ensembl
chr14:48690936..48709792hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3818857
hg1918857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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