A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132851



Internal ID21415838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28520965..28520965hg38UCSC Ensembl
chr4:28522587..28522587hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616616
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132851
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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