A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065408



Internal ID21407902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51580899..51580953hg38UCSC Ensembl
chr1:52046571..52046625hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567302
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065408
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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