A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117118



Internal ID21300384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:11589462..11602154hg38UCSC Ensembl
Innerchr6:11589695..11602387hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg3812693
hg1912693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083027
Samplessample342
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117118
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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