A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877350



Internal ID22652314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205647158..205648088hg38UCSC Ensembl
chr1:205616286..205617216hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38931
hg19931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv117n209
Supporting Variantsnssv17357255
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877350
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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