A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062818



Internal ID21510225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222488559..222489413hg38UCSC Ensembl
chr1:222661901..222662755hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572525
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062818
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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