A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447223



Internal ID21104776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109294526..109302964hg38UCSC Ensembl
chr9:112056806..112065244hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg388439
hg198439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173147
Samples
Known GenesEPB41L4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447223
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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