A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447043



Internal ID21104596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111905663..111913715hg38UCSC Ensembl
chr9:114667943..114675995hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg388053
hg198053
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233666
Samples
Known GenesUGCG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447043
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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