A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885207



Internal ID22660192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151510282..151511119hg38UCSC Ensembl
chr1:151482758..151483595hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38838
hg19838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357087
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885207
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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