A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882056



Internal ID22657033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32776178..32778768hg38UCSC Ensembl
chr1:33241779..33244369hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg382591
hg192591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379405
Samples
Known GenesYARS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882056
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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