A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451544



Internal ID21109097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93376330..93376643hg38UCSC Ensembl
chr9:96138612..96138925hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193513
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451544
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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