A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17102111



Internal ID21454466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76997751..76997823hg38UCSC Ensembl
chr18:74709707..74709779hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588089
Supporting Variants
SamplesHG02011
Known GenesMBP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17102111
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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