A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624012



Internal ID21816059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6620538..6662548hg38UCSC Ensembl
chr18:6620537..6662547hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3842011
hg1942011
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038122
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624012
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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