A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001092



Internal ID21910435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:111531934..111531994hg38UCSC Ensembl
chr5:110867632..110867692hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546581
Samples
Known GenesSTARD4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001092
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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