A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016930



Internal ID21926273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151450001..151454711hg38UCSC Ensembl
chr5:150829562..150834272hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg384711
hg194711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558057
Samples
Known GenesSLC36A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016930
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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