A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17064303



Internal ID21489626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26334743..26335296hg38UCSC Ensembl
chr1:26661234..26661787hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575741
Supporting Variants
SamplesNA18939
Known GenesAIM1L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17064303
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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