A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214679



Internal ID20781720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32097701..32121000hg38UCSC Ensembl
chr4:32099323..32122622hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3823300
hg1923300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369937
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214679
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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