A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491093



Internal ID21148646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:82361270..82383073hg38UCSC Ensembl
chr14:82827614..82849417hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3821804
hg1921804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491093
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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