A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502172



Internal ID20875414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104308938..104548367hg38UCSC Ensembl
chr14:104775275..105014704hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38239430
hg19239430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015972
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502172
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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