A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061567



Internal ID21464089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165473440..165473504hg38UCSC Ensembl
chr1:165442677..165442741hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5576730
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061567
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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