A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117055



Internal ID21300321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178966654..178982241hg38UCSC Ensembl
Innerchr5:178393655..178409242hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3815588
hg1915588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14082615
Samplessample380
Known GenesGRM6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117055
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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