A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454541



Internal ID21112094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133027143..133038647hg38UCSC Ensembl
chr9:135902530..135914034hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3811505
hg1911505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177079
Samples
Known GenesGTF3C5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454541
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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