A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480947



Internal ID21138500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24200610..24205472hg38UCSC Ensembl
chr14:24669816..24674678hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg384863
hg194863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016800
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480947
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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