A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487259



Internal ID21144812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:40128698..40299952hg38UCSC Ensembl
chr14:40597902..40769156hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38171255
hg19171255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018377
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487259
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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