A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201795



Internal ID20768835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:187122200..187165482hg38UCSC Ensembl
chr1:187091332..187134614hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3843283
hg1943283
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333090
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201795
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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