A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868233



Internal ID22643168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32952570..32955558hg38UCSC Ensembl
chr1:33418171..33421159hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg382989
hg192989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381736
Samples
Known GenesRNF19B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868233
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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