A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201620



Internal ID20768661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168902816..168904224hg38UCSC Ensembl
chr1:168872054..168873462hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg381409
hg191409
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319024
Supporting Variants
Samples
Known GenesLINC00970
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201620
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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