A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489199



Internal ID21146752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34412207..34413437hg38UCSC Ensembl
chr14:34881413..34882643hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg381231
hg191231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017406
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489199
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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