A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425163



Internal ID21082716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80624205..80656517hg38UCSC Ensembl
chr8:81536440..81568752hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3832313
hg1932313
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222489
Samples
Known GenesZNF704
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425163
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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