A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887516



Internal ID22662508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:191477881..191739211hg38UCSC Ensembl
chr1:191447011..191708341hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38261331
hg19261331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887516
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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