A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887054



Internal ID22662045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221205778..221209164hg38UCSC Ensembl
chr1:221379120..221382506hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg383387
hg193387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887054
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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