A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202375



Internal ID20769415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:233424185..233430680hg38UCSC Ensembl
chr1:233559931..233566426hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg386496
hg196496
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331074
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202375
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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