A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441534



Internal ID21099087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114139782..114146264hg38UCSC Ensembl
chr9:116902062..116908544hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg386483
hg196483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174451
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441534
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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