A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636546



Internal ID21828593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:57120108..57120108hg38UCSC Ensembl
chr18:54787339..54787339hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6100890
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636546
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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