A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434392



Internal ID21396394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55960921..55961766hg38UCSC Ensembl
chr4:56827087..56827932hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38846
hg19846
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15754609
SamplesMDQ010
Known GenesCEP135
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434392
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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