A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15745817



Internal ID21387189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101039000..101040030hg38UCSC Ensembl
chr4:101960157..101961187hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg381031
hg191031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434129
Supporting Variants
SamplesMDQ025
Known GenesPPP3CA
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15745817
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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