A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434148



Internal ID21396150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:110418681..110425941hg38UCSC Ensembl
chr4:111339837..111347097hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg387261
hg197261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15747250
SamplesNB07
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434148
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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