A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14084229



Internal ID21269164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:121394875..121396814hg38UCSC Ensembl
Innerchr7:121034929..121036868hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg381940
hg191940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114564
Supporting Variants
Samplessample136
Known GenesFAM3C
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14084229
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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