A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496519



Internal ID20869722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98327490..98327972hg38UCSC Ensembl
chr14:98793827..98794309hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023085
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496519
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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