A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101062



Internal ID21483284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23277265..23280807hg38UCSC Ensembl
chr18:20857229..20860771hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383543
hg193543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602017
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101062
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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