A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368891



Internal ID21026444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:1099328..2170151hg38UCSC Ensembl
chr3:1141012..2211835hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg381070824
hg191070824
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4750n223
Supporting Variantsnssv18207232
Samples
Known GenesCNTN4, CNTN4-AS2, CNTN6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368891
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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