A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059816



Internal ID21463005
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 StatusS
Merged Variantsnsv5567675
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17059816
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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