A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155303



Internal ID22085808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3019916..3291811hg38UCSC Ensembl
Outerchr1:3018452..3296382hg38UCSC Ensembl
Innerchr1:2936480..3208375hg19UCSC Ensembl
Outerchr1:2935016..3212946hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38277931
hg19277931
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4012203
Samples
Known GenesACTRT2, LINC00982, MIR4251, PRDM16
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155303
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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