A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626629



Internal ID15850162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:65774191..65777949hg38UCSC Ensembl
Outerchr4:66639909..66643667hg19UCSC Ensembl
Outerchr4:66322504..66326262hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg383759
hg193759
hg183759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513136
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)nssv626629
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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