A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061446



Internal ID21509942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180882710..180882710hg38UCSC Ensembl
chr1:180851846..180851846hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg381189
hg191189
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619148
Supporting Variants
SamplesNA20847
Known GenesXPR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061446
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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