A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425106



Internal ID21082659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77631070..77894456hg38UCSC Ensembl
chr8:78543306..78806691hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38263387
hg19263386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170442
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425106
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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