A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513139



Internal ID15505875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:76043096..76051162hg38UCSC Ensembl
Outerchr4:76964249..76972315hg19UCSC Ensembl
Outerchr4:77183273..77191339hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg388067
hg198067
hg188067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626633
Samples1
Known GenesART3
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513139
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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