A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905252



Internal ID22680437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138940305..138992833hg38UCSC Ensembl
chr4:139861459..139913987hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3852529
hg1952529
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416860
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905252
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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