A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886603



Internal ID22661592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93952388..93952489hg38UCSC Ensembl
chr1:94417944..94418045hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401659
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886603
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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