A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497219



Internal ID20870424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100191521..100195500hg38UCSC Ensembl
chr14:100657858..100661837hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg383980
hg193980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016445
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497219
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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