A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17134251



Internal ID21497859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3051815..3051815hg38UCSC Ensembl
chr4:3053542..3053542hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5612223
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17134251
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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