A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117541



Internal ID21462653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6049842..6049842hg38UCSC Ensembl
chr20:6030488..6030488hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651876
Supporting Variants
SamplesHG03009
Known GenesLRRN4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117541
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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