A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893811



Internal ID22668876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155194161..155194285hg38UCSC Ensembl
chr4:156115313..156115437hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418658
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893811
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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