A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997341



Internal ID21906684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48416519..48416638hg38UCSC Ensembl
chr4:48418536..48418655hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556454
Samples
Known GenesSLAIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997341
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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