A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606056



Internal ID20979127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158750893..158753179hg38UCSC Ensembl
chr6:159171925..159174211hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382287
hg192287
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216710
Samples
Known GenesSYTL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606056
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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