A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441784



Internal ID21099337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65548601..65584900hg38UCSC Ensembl
chr9:44825291..44861733hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3836300
hg1936443
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228467
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441784
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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