A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137846



Internal ID20704886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:129594801..129596500hg38UCSC Ensembl
chr6:129915946..129917645hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605996
Supporting Variants
Samples
Known GenesARHGAP18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137846
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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