A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114534



Internal ID21297800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16384197..16499694hg38UCSC Ensembl
Innerchr1:16710692..16826189hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38115498
hg19115498
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090885
Samplessample273
Known GenesCROCCP3, NECAP2, SPATA21, SZRD1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114534
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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