A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445815



Internal ID21103368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:103627939..103789700hg38UCSC Ensembl
chr9:106390221..106551981hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38161762
hg19161761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172554
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445815
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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