A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505966



Internal ID20879241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91072231..91092964hg38UCSC Ensembl
chr14:91538575..91559308hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3820734
hg1920734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022730
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505966
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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