A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396427



Internal ID21053980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20882023..20882592hg38UCSC Ensembl
chr6:20882254..20882823hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38570
hg19570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139960
Samples
Known GenesCDKAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396427
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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