A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155991



Internal ID22086496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:82807604..82831894hg38UCSC Ensembl
Outerchr3:82806586..82833626hg38UCSC Ensembl
Innerchr3:82856755..82881045hg19UCSC Ensembl
Outerchr3:82855737..82882777hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3827041
hg1927041
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4017627
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155991
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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