A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602170



Internal ID20975241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:129582551..129583274hg38UCSC Ensembl
chr6:129903696..129904419hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137843
Samples
Known GenesARHGAP18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602170
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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