A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199759



Internal ID20766799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11758997..11763235hg38UCSC Ensembl
chr1:11819054..11823292hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg384239
hg194239
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326393
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199759
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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