A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886253



Internal ID22661239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84609351..84609436hg38UCSC Ensembl
chr1:85075034..85075119hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886253
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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