A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625228



Internal ID15502078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:41277050..41279155hg38UCSC Ensembl
Outerchr20:39905690..39907795hg19UCSC Ensembl
Outerchr20:39339104..39341209hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg382106
hg192106
hg182106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512615
Supporting Variants
Samples1
Known GenesZHX3
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625228
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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