A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367194



Internal ID21024747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98488607..99037059hg38UCSC Ensembl
chr3:98207451..98755903hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38548453
hg19548453
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211290
Samples
Known GenesCLDND1, CPOX, DCBLD2, GPR15, OR5K2, ST3GAL6, ST3GAL6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367194
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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