A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155503



Internal ID22086008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11769448..11779858hg38UCSC Ensembl
Outerchr18:11767732..11781077hg38UCSC Ensembl
Innerchr18:11769447..11779857hg19UCSC Ensembl
Outerchr18:11767731..11781076hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3813346
hg1913346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011885
Samples
Known GenesGNAL
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155503
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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