A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997525



Internal ID21906868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48412311..48412532hg38UCSC Ensembl
chr4:48414328..48414549hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557527
Samples
Known GenesSLAIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997525
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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