A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426220



Internal ID21083773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18490369..18581495hg38UCSC Ensembl
chr9:18490367..18581493hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3891127
hg1991127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223834
Samples
Known GenesADAMTSL1, MIR3152
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426220
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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