A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213996



Internal ID20781036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:4771954..4787031hg38UCSC Ensembl
chr5:4772067..4787144hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3815078
hg1915078
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6394642
Supporting Variants
Samples
Known GenesLOC101929153
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213996
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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