A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063684



Internal ID21510663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244190661..244190710hg38UCSC Ensembl
chr1:244353963..244354012hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581874
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063684
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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