A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061141



Internal ID21482038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150612667..150621524hg38UCSC Ensembl
chr1:150585143..150594000hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg388858
hg198858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582613
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061141
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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