A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746915



Internal ID20522931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47976145..47976271hg38UCSC Ensembl
chr4:47978162..47978288hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285199
Samples
Known GenesCNGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746915
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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