A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127847



Internal ID21511713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10548..10548hg38UCSC Ensembl
chr18:10272..10272hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622516
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127847
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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