A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454363



Internal ID21111916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100811134..100811259hg38UCSC Ensembl
chr9:103573416..103573541hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171580
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454363
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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