A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397879



Internal ID21055432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80796601..80800900hg38UCSC Ensembl
chr6:81506318..81510617hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144569
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397879
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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