A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101443



Internal ID21476672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45694181..45694181hg38UCSC Ensembl
chr18:43274146..43274146hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654909
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101443
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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