A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17133417



Internal ID21416070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56719966..56719966hg38UCSC Ensembl
chr3:56753994..56753994hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608320
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17133417
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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