A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416328



Internal ID21073881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80493341..80719587hg38UCSC Ensembl
chr8:81405576..81631822hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38226247
hg19226247
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233054
Samples
Known GenesZBTB10, ZNF704
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416328
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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