A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060943



Internal ID20627983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32902298..32904203hg38UCSC Ensembl
chr1:33367899..33369804hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381906
hg191906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6315869
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060943
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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