A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626607



Internal ID15850140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:1601097..1602318hg38UCSC Ensembl
Outerchr4:1602824..1604045hg19UCSC Ensembl
Outerchr4:1572784..1574005hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381222
hg191222
hg181222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513116
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)nssv626607
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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