A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894467



Internal ID22669539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145353204..145368862hg38UCSC Ensembl
chr4:146274356..146290014hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3815659
hg1915659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894467
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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