A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155974



Internal ID22086479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:74559478..74818266hg38UCSC Ensembl
Outerchr3:74553236..74825622hg38UCSC Ensembl
Innerchr3:74608629..74867417hg19UCSC Ensembl
Outerchr3:74602387..74874773hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38272387
hg19272387
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016407
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155974
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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