A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061559



Internal ID21476016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165246820..165246820hg38UCSC Ensembl
chr1:165216057..165216057hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616970
Supporting Variants
SamplesHG03486
Known GenesLMX1A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061559
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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