A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101146



Internal ID21499689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34790341..34790559hg38UCSC Ensembl
chr18:32370305..32370523hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602573
Supporting Variants
SamplesNA19239
Known GenesDTNA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101146
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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