A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392412



Internal ID21049965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97433301..97485900hg38UCSC Ensembl
chr4:98354452..98407051hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3852600
hg1952600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5380n223
Supporting Variantsnssv18214383
Samples
Known GenesSTPG2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392412
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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