A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513161



Internal ID15505897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:112576913..112581808hg38UCSC Ensembl
Outerchr4:113498069..113502964hg19UCSC Ensembl
Outerchr4:113717518..113722413hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg384896
hg194896
hg184896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626657
Samples1
Known GenesC4orf21
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513161
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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