A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734473



Internal ID20510409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48412311..48412533hg38UCSC Ensembl
chr4:48414328..48414550hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292630
Samples
Known GenesSLAIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734473
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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