A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886082



Internal ID22661068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:79699364..79706833hg38UCSC Ensembl
chr1:80165049..80172518hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg387470
hg197470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387647
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886082
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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