A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120645



Internal ID21473881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155824013..155824013hg38UCSC Ensembl
chr3:155541802..155541802hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg381050
hg191050
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613150
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120645
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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