A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215911



Internal ID20782951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157136790..157140751hg38UCSC Ensembl
chr5:156563801..156567762hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg383962
hg193962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407095
Supporting Variants
Samples
Known GenesMED7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215911
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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