A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205520



Internal ID20772560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:150158701..150184600hg38UCSC Ensembl
chr2:151015215..151041114hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg3825900
hg1925900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350338
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205520
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00014


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