A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884856



Internal ID22659840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:188022639..188077609hg38UCSC Ensembl
chr1:187991770..188046740hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3854971
hg1954971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364326
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884856
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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