A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100709



Internal ID21493209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:30543023..30543094hg38UCSC Ensembl
chr18:28122989..28123060hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600605
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100709
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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