A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200965



Internal ID20768005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159272903..159273798hg38UCSC Ensembl
chr1:159242693..159243588hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38896
hg19896
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329648
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200965
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00292


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