A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901071



Internal ID22676219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1853157..1853209hg38UCSC Ensembl
chr4:1854884..1854936hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412853
Samples
Known GenesLETM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901071
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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