A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113162



Internal ID21296428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:95489181..95495157hg38UCSC Ensembl
Innerchr7:95118493..95124469hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg385977
hg195977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085417
Samplessample250
Known GenesASB4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113162
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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