A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365704



Internal ID21023257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:5532313..5564822hg38UCSC Ensembl
chr4:5534040..5566549hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3832510
hg1932510
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211945
Samples
Known GenesEVC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365704
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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