A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434728



Internal ID21396730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111720798..111874797hg38UCSC Ensembl
chr6:112042001..112196000hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38154000
hg19154000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749336
SamplesSMI041
Known GenesFYN
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434728
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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