A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567675



Internal ID21516013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117777908..117779214hg38UCSC Ensembl
chr1:118320530..118321836hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg381307
hg191307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17059816
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567675
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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