A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060016



Internal ID21501413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12062838..12062838hg38UCSC Ensembl
chr1:12122895..12122895hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610696
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060016
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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