A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434404



Internal ID21396406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67087918..67096559hg38UCSC Ensembl
chr4:67953636..67962277hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg388642
hg198642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749469
SamplesSMI034
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434404
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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