A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535018



Internal ID310735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52733432..52733452hg38UCSC Ensembl
chr4:53599599..53599619hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16950045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535018
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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