A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492596



Internal ID21150149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87134159..87134592hg38UCSC Ensembl
chr14:87600503..87600936hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022391
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492596
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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