A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616078



Internal ID20989149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:129632510..129758391hg38UCSC Ensembl
chr6:129953655..130079536hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38125882
hg19125882
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215538
Samples
Known GenesARHGAP18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616078
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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