A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609656



Internal ID20982727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:129665120..129708432hg38UCSC Ensembl
chr6:129986265..130029577hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg3843313
hg1943313
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215539
Samples
Known GenesARHGAP18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609656
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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