A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881313



Internal ID22656288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:80376337..80377757hg38UCSC Ensembl
chr1:80842022..80843442hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg381421
hg191421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379107
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881313
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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