A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053677



Internal ID20620717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169401200..169402674hg38UCSC Ensembl
chr1:169370438..169371912hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg381475
hg191475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332420
Supporting Variants
Samples
Known GenesCCDC181
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053677
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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