A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066580



Internal ID21434714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:79648487..79648803hg38UCSC Ensembl
chr1:80114172..80114488hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569021
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066580
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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