A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535378



Internal ID20908739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6867375..6896323hg38UCSC Ensembl
chr18:6867374..6896322hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3828949
hg1928949
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197610
Samples
Known GenesARHGAP28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535378
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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