A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432012



Internal ID21089565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23978867..23983548hg38UCSC Ensembl
chr8:23836380..23841061hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg384682
hg194682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167166
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432012
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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