A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17064304



Internal ID21433764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26345014..26345064hg38UCSC Ensembl
chr1:26671505..26671555hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584304
Supporting Variants
SamplesHG00731
Known GenesAIM1L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17064304
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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