A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207214



Internal ID20774255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108755301..109193900hg38UCSC Ensembl
chr3:108474148..108912747hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38438600
hg19438600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365771
Supporting Variants
Samples
Known GenesFLJ22763, GUCA1C, LINC00488, MORC1, RETNLB, TRAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207214
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00064


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