A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391606



Internal ID21382636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168881455..168881541hg38UCSC Ensembl
chr4:169802606..169802692hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9n171
Supporting Variantsnssv15703310
Samples
Known GenesPALLD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391606
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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