A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442391



Internal ID21099944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66237901..66300800hg38UCSC Ensembl
chr9:42220872..42283309hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3862900
hg1962438
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233625
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442391
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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