A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205437



Internal ID20772477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19163946..19538550hg38UCSC Ensembl
chr2:19363707..19738311hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38374605
hg19374605
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6352960
Supporting Variants
Samples
Known GenesMIR4757, OSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205437
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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