A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369551



Internal ID21027104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9367601..9386300hg38UCSC Ensembl
chr4:9369327..9388026hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3818700
hg1918700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215355
Samples
Known GenesUSP17L6P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369551
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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