A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411206



Internal ID21068759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4921507..4924240hg38UCSC Ensembl
chr6:4921741..4924474hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg382734
hg192734
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225011
Samples
Known GenesCDYL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411206
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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