A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418183



Internal ID21075736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16962532..16992747hg38UCSC Ensembl
chr9:16962530..16992745hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3830216
hg1930216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174741
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418183
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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