A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065869



Internal ID21975102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53477869..53477869hg38UCSC Ensembl
chr4:54344036..54344036hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542906
Samples
Known GenesLNX1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065869
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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