A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748065



Internal ID21392098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1116046..1119678hg38UCSC Ensembl
chr4:1109834..1113466hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg383633
hg193633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434147
Supporting Variants
SamplesSMI034
Known GenesTMED11P
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748065
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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