A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889383



Internal ID22664400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145826765..145826814hg38UCSC Ensembl
chr4:146747917..146747966hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426708
Samples
Known GenesZNF827
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889383
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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