A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215227



Internal ID20782267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8973501..9156400hg38UCSC Ensembl
chr4:8975227..9158126hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38182900
hg19182900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363409
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215227
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03263


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