A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885167



Internal ID22660152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51558019..51562946hg38UCSC Ensembl
chr1:52023691..52028618hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg384928
hg194928
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376841
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885167
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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