A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17102968



Internal ID21460083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79684903..79684981hg38UCSC Ensembl
chr18:77444903..77444981hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591271
Supporting Variants
SamplesHG02818
Known GenesCTDP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17102968
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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