A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416071



Internal ID21073624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26462995..26463581hg38UCSC Ensembl
chr8:26320511..26321097hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38587
hg19587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416071
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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