A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892067



Internal ID22667112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:110439075..110439233hg38UCSC Ensembl
chr4:111360231..111360389hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418300
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892067
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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