A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867900



Internal ID22642835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62440106..62440376hg38UCSC Ensembl
chr1:62905777..62906047hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383669
Samples
Known GenesUSP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867900
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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