A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053626



Internal ID20620666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168924659..168925136hg38UCSC Ensembl
chr1:168893897..168894374hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318382
Supporting Variants
Samples
Known GenesLINC00970
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053626
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00045


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