A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885305



Internal ID22660289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110288876..110288926hg38UCSC Ensembl
chr1:110831498..110831548hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355525
Samples
Known GenesLOC440600
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885305
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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