A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073941



Internal ID21983174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101808854..101808854hg38UCSC Ensembl
chr3:101527698..101527698hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538219
Samples
Known GenesNXPE3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073941
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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