A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114804



Internal ID21298070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143435017..143447734hg38UCSC Ensembl
Innerchr7:143132110..143144827hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3812718
hg1912718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085574
Samplessample288
Known GenesEPHA1-AS1, TAS2R60
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114804
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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