A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214728



Internal ID20781768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83584801..83604000hg38UCSC Ensembl
chr4:84505954..84525153hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3819200
hg1919200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6388721
Supporting Variants
Samples
Known GenesAGPAT9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214728
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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