A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877953



Internal ID22652919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117050785..117052321hg38UCSC Ensembl
chr1:117593407..117594943hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg381537
hg191537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361631
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877953
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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