A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058874



Internal ID20625914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235613612..235615244hg38UCSC Ensembl
chr1:235776912..235778544hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg381633
hg191633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331929
Supporting Variants
Samples
Known GenesGNG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058874
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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