A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427498



Internal ID21085051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66113422..66113507hg38UCSC Ensembl
chr8:67025657..67025742hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229355
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427498
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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