A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875815



Internal ID22650773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101855869..101861371hg38UCSC Ensembl
chr1:102321425..102326927hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg385503
hg195503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357767
Samples
Known GenesOLFM3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875815
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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