A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568772



Internal ID21517122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:121257176..121364377hg38UCSC Ensembl
chr1:143985979..144073867hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38107202
hg1987889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17060883
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568772
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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