A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477204



Internal ID21134757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81410101..81414200hg38UCSC Ensembl
chr14:81876445..81880544hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021400
Samples
Known GenesSTON2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477204
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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