A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477615



Internal ID21135168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:48255492..48268204hg38UCSC Ensembl
chr14:48724695..48737407hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3812713
hg1912713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019499
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477615
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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