A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443049



Internal ID21100602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64315501..64351700hg38UCSC Ensembl
chr9:69328386..69364118hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3836200
hg1935733
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221229
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443049
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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