A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112261



Internal ID21295527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:92447186..92448876hg38UCSC Ensembl
Innerchr7:92076500..92078190hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg381691
hg191691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14084228
Samplessample136
Known GenesGATAD1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112261
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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