A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446220



Internal ID21103773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73452062..73465339hg38UCSC Ensembl
chr9:76066978..76080255hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3813278
hg1913278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446220
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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