A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14084783



Internal ID21284287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:50346933..50350825hg38UCSC Ensembl
Innerchr7:50414631..50418523hg19UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg383893
hg193893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113306
Supporting Variants
Samplessample36
Known GenesIKZF1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14084783
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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