A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440940



Internal ID21098493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112391677..112452518hg38UCSC Ensembl
chr9:115153957..115214798hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3860842
hg1960842
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220468
Samples
Known GenesHSDL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440940
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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