A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886031



Internal ID22661018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96294234..96295778hg38UCSC Ensembl
chr1:96759790..96761334hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg381545
hg191545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886031
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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