A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211837



Internal ID20778877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:27415801..27473200hg38UCSC Ensembl
chr4:27417423..27474822hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3857400
hg1957400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369832
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211837
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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