A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17538367



Internal ID21862722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17374135..17374135hg38UCSC Ensembl
chr4:17375758..17375758hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6079920
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17538367
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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