A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155506



Internal ID22086011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:37919692..37955722hg38UCSC Ensembl
Outerchr18:37916686..37956604hg38UCSC Ensembl
Innerchr18:35499656..35535686hg19UCSC Ensembl
Outerchr18:35496650..35536568hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3839919
hg1939919
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011888
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155506
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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