A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451924



Internal ID21109477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107388994..107389999hg38UCSC Ensembl
chr9:110151275..110152280hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381006
hg191006
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173402
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451924
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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