A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440791



Internal ID21098344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121790001..121796400hg38UCSC Ensembl
chr9:124552280..124558679hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176345
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440791
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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