A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006339



Internal ID21915682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139139816..139139958hg38UCSC Ensembl
chr5:138475505..138475647hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551379
Samples
Known GenesSIL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006339
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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