A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434542



Internal ID21396544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157850396..157851594hg38UCSC Ensembl
chr5:157277404..157278602hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg381199
hg191199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15748234
SamplesMDQ010
Known GenesCLINT1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434542
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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