A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757169



Internal ID20533029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53578930..53578930hg38UCSC Ensembl
chr4:54445097..54445097hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273909
Samples
Known GenesLNX1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757169
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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