A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010179



Internal ID21919522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147561367..147561424hg38UCSC Ensembl
chr5:146940930..146940987hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574833
Samples
Known GenesJAKMIP2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010179
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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