A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18054345



Internal ID20621386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:187106016..187151577hg38UCSC Ensembl
chr1:187075148..187120709hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3845562
hg1945562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335000
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18054345
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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