A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411305



Internal ID21068858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85650228..85666592hg38UCSC Ensembl
chr6:86359946..86376310hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3816365
hg1916365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146066
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411305
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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