A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422174



Internal ID21079727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132046003..132050427hg38UCSC Ensembl
chr8:133058250..133062674hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg384425
hg194425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165675
Samples
Known GenesOC90
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422174
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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