A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063018



Internal ID21972251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48455203..48455203hg38UCSC Ensembl
chr4:48457220..48457220hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548844
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063018
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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