A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058574



Internal ID20625614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229931901..229932300hg38UCSC Ensembl
chr1:230067648..230068047hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335104
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058574
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02142


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