A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438907



Internal ID21096460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40911345..40930876hg38UCSC Ensembl
chr9:68988947..69004105hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3819532
hg1915159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7716n223
Supporting Variantsnssv18227945
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438907
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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