A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200491



Internal ID20767531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153716819..153726842hg38UCSC Ensembl
chr1:153689295..153699318hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3810024
hg1910024
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334074
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200491
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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