A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373976



Internal ID21031529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:144260078..144283831hg38UCSC Ensembl
chr3:143978920..144002673hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3823754
hg1923754
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209678
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373976
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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