A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422147



Internal ID21079700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37819875..37824162hg38UCSC Ensembl
chr8:37677393..37681680hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg384288
hg194288
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219616
Samples
Known GenesGPR124
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422147
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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