A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901303



Internal ID22676453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140302934..140302987hg38UCSC Ensembl
chr4:141224088..141224141hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428364
Samples
Known GenesLOC100129858, SCOC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901303
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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