A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436147



Internal ID21093700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80017871..80027870hg38UCSC Ensembl
chr9:82632786..82642785hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3810000
hg1910000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227447
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436147
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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