A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610809



Internal ID20983880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106089361..106121386hg38UCSC Ensembl
chr7:105729807..105761832hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3832026
hg1932026
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221190
Samples
Known GenesSYPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610809
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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