A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066085



Internal ID21451057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:69530707..69537018hg38UCSC Ensembl
chr1:69996390..70002701hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg386312
hg196312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580698
Supporting Variants
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066085
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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