A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128349



Internal ID21487787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38219333..38219333hg38UCSC Ensembl
chr4:38220954..38220954hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622450
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128349
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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