A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419997



Internal ID21077550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42735099..42744119hg38UCSC Ensembl
chr8:42590242..42599262hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg389021
hg199021
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234639
Samples
Known GenesCHRNB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419997
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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