A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427574



Internal ID21085127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22293391..22364669hg38UCSC Ensembl
chr8:22150904..22222182hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3871279
hg1971279
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225491
Samples
Known GenesPIWIL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427574
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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