A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878861



Internal ID22653827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:123507489..124389657hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38882169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv66n209
Supporting Variantsnssv17356376
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878861
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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