A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365145



Internal ID21022698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138639681..139021588hg38UCSC Ensembl
chr3:138358523..138740430hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38381908
hg19381908
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209619
Samples
Known GenesC3orf72, FOXL2, PIK3CB, PRR23A, PRR23B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365145
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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