A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610867



Internal ID20983938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117372701..117378100hg38UCSC Ensembl
chr6:117693864..117699263hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214538
Samples
Known GenesROS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610867
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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