A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871077



Internal ID22646015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:113978319..113982836hg38UCSC Ensembl
chr1:114520941..114525458hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg384518
hg194518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354148
Samples
Known GenesOLFML3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871077
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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