A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365946



Internal ID21023499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140902265..140903516hg38UCSC Ensembl
chr3:140621107..140622358hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381252
hg191252
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209636
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365946
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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