A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209509



Internal ID20776549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108722923..108787555hg38UCSC Ensembl
chr4:109644079..109708711hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3864633
hg1964633
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390953
Supporting Variants
Samples
Known GenesETNPPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209509
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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