A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486768



Internal ID21144321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27080323..27292153hg38UCSC Ensembl
chr14:27549529..27761359hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38211831
hg19211831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486768
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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