A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444578



Internal ID21102131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33830452..33833281hg38UCSC Ensembl
chr9:33830450..33833279hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg382830
hg192830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182471
Samples
Known GenesUBE2R2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444578
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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