A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118297



Internal ID21301563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:78137232..78370805hg38UCSC Ensembl
Innerchr1:78602916..78836490hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38233574
hg19233575
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099694
Samplessample392
Known GenesGIPC2, MGC27382
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118297
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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