A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113625



Internal ID21296891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:90855223..90860200hg38UCSC Ensembl
Innerchr10:92614980..92619957hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg384978
hg194978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv171n145
Supporting Variantsnssv14088709
Samplessample273
Known GenesHTR7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113625
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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