A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621191



Internal ID21813238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70649699..70649699hg38UCSC Ensembl
chr18:68316935..68316935hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112057
Supporting Variants
Samples
Known GenesGTSCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621191
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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