A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114785



Internal ID21298051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16597790..16875287hg38UCSC Ensembl
Innerchr1:16924285..17201782hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38277498
hg19277498
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104808
Samplessample52
Known GenesCROCCP2, ESPNP, LOC729574, MIR3675, MST1L, MST1P2, NBPF1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114785
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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