A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2798492



Internal ID21243830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:626930..626989hg38UCSC Ensembl
chr18:626930..626989hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13685513
Samples
Known GenesCLUL1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2798492
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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