A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113761



Internal ID21297027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:108777227..108845960hg38UCSC Ensembl
Innerchr7:108417671..108486404hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3868734
hg1968734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085530
Samplessample276
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113761
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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