A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112305



Internal ID21295571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88241621..88248371hg38UCSC Ensembl
Innerchr9:90856536..90863286hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg386751
hg196751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086891
Samplessample218
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112305
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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