A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443882



Internal ID21101435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41049801..41130700hg38UCSC Ensembl
chr9:70915540..70986000hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3880900
hg1970461
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7720n223
Supporting Variantsnssv18227065
Samples
Known GenesFOXD4L3, PGM5, PGM5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443882
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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