A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904292



Internal ID22679469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:143702631..143720974hg38UCSC Ensembl
chr4:144623784..144642127hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3818344
hg1918344
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425198
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904292
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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