A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361170



Internal ID21018723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28246405..28248721hg38UCSC Ensembl
chr3:28287896..28290212hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg382317
hg192317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210478
Samples
Known GenesCMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361170
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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