A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112595



Internal ID21295861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:112672605..112677726hg38UCSC Ensembl
Innerchr1:113215227..113220348hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg385122
hg195122
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099263
Samplessample360
Known GenesMOV10
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112595
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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