A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368900



Internal ID21026453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:50236772..50288786hg38UCSC Ensembl
chr3:50274204..50326217hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3852015
hg1952014
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209373
Samples
Known GenesGNAI2, IFRD2, LSMEM2, MIR6872, SEMA3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368900
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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