A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610789



Internal ID20983860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110965366..110988758hg38UCSC Ensembl
chr6:111286569..111309961hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3823393
hg1923393
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216812
Samples
Known GenesGTF3C6, RPF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610789
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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