A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625624



Internal ID21817671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31284216..31289545hg38UCSC Ensembl
chr18:28864179..28869508hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg385330
hg195330
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023434
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625624
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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