A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610597



Internal ID20983668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105174296..105195914hg38UCSC Ensembl
chr6:105622171..105643789hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3821619
hg1921619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216546
Samples
Known GenesPOPDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610597
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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