A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110346



Internal ID21293612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155295188..155299671hg38UCSC Ensembl
Innerchr7:155086898..155091381hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg384484
hg194484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1151n145
Supporting Variantsnssv14083374
Samplessample93
Known GenesINSIG1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110346
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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