A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418947



Internal ID21076500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28772318..28774775hg38UCSC Ensembl
chr8:28629835..28632292hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg382458
hg192458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166180
Samples
Known GenesINTS9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418947
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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