A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399684



Internal ID21057237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80874923..80915861hg38UCSC Ensembl
chr6:81584640..81625578hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3840939
hg1940939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6293n223
Supporting Variantsnssv18144584
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399684
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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