A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419051



Internal ID21076604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32765720..32977167hg38UCSC Ensembl
chr8:32623238..32834685hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38211448
hg19211448
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236444
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419051
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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