A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358798



Internal ID21016351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9367601..9405900hg38UCSC Ensembl
chr4:9369327..9407626hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3838300
hg1938300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215356
Samples
Known GenesUSP17L6P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358798
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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