A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059940



Internal ID21431946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111544741..111544910hg38UCSC Ensembl
chr1:112087363..112087532hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5573976
Supporting Variants
SamplesHG00731
Known GenesADORA3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17059940
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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