A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356694



Internal ID21014247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3025398..3036228hg38UCSC Ensembl
chr4:3027125..3037955hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3810831
hg1910831
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214654
Samples
Known GenesGRK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356694
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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