A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065142



Internal ID21974375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57301057..57301057hg38UCSC Ensembl
chr5:56596884..56596884hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539159
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065142
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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