A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427545



Internal ID21085098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41638389..41646931hg38UCSC Ensembl
chr8:41495908..41504450hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg388543
hg198543
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222483
Samples
Known GenesNKX6-3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427545
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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