A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736843



Internal ID20512796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138537918..138538304hg38UCSC Ensembl
chr5:137873607..137873993hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291452
Samples
Known GenesETF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736843
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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