A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904539



Internal ID22679716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152174465..152175221hg38UCSC Ensembl
chr4:153095617..153096373hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38757
hg19757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1604n209
Supporting Variantsnssv17419553
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904539
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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