A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625215



Internal ID15848751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:7115577..7122247hg38UCSC Ensembl
Outerchr20:7096224..7102894hg19UCSC Ensembl
Outerchr20:7044224..7050894hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg386671
hg196671
hg186671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512603
Supporting Variants
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625215
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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