A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113847



Internal ID21297113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40641642..40709304hg38UCSC Ensembl
Innerchr7:40681241..40748903hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3867663
hg1967663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085013
Samplessample403
Known GenesC7orf10
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113847
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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