A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476942



Internal ID21134495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:56421644..56425390hg38UCSC Ensembl
chr14:56888362..56892108hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg383747
hg193747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476942
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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