A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347241



Internal ID21004794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:12585..244020hg38UCSC Ensembl
chr3:60001..285703hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38231436
hg19225703
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4740n223
Supporting Variantsnssv18208448
Samples
Known GenesCHL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347241
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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