A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209505



Internal ID20776545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107931001..107932600hg38UCSC Ensembl
chr4:108852157..108853756hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395341
Supporting Variants
Samples
Known GenesCYP2U1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209505
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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