A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131226



Internal ID21453389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141541767..141541767hg38UCSC Ensembl
chr4:142462920..142462920hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5623058
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131226
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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