A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624753



Internal ID21816800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78809877..78810030hg38UCSC Ensembl
chr18:76569877..76570030hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026034
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624753
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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