A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899478



Internal ID22674608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:19031096..19356506hg38UCSC Ensembl
chr4:19032719..19358129hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38325411
hg19325411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413417
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899478
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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