A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607991



Internal ID20981062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:129587703..129596354hg38UCSC Ensembl
chr6:129908848..129917499hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg388652
hg198652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137845
Samples
Known GenesARHGAP18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607991
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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