A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399899



Internal ID21057452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14114825..14118543hg38UCSC Ensembl
chr6:14115056..14118774hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg383719
hg193719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140404
Samples
Known GenesCD83
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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