A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483836



Internal ID21141389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:40318701..40320100hg38UCSC Ensembl
chr14:40787905..40789304hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018411
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483836
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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