A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602199



Internal ID20975270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106095987..106305657hg38UCSC Ensembl
chr6:106543862..106753532hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38209671
hg19209671
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216554
Samples
Known GenesATG5, PRDM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602199
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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