A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440226



Internal ID21097779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79083355..79099169hg38UCSC Ensembl
chr9:81698271..81714085hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3815815
hg1915815
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225373
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440226
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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