A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112636



Internal ID21295902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:3712496..3719286hg38UCSC Ensembl
Innerchr6:3712730..3719520hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg386791
hg196791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087661
Samplessample208
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112636
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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