A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420574



Internal ID21078127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27045823..27052765hg38UCSC Ensembl
chr8:26903340..26910282hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg386943
hg196943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166095
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420574
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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