A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094782



Internal ID21285181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:146306707..146339335hg38UCSC Ensembl
Innerchr4:147227859..147260487hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3832629
hg1932629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117222
Supporting Variants
Samplessample370
Known GenesSLC10A7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094782
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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