A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512038



Internal ID15851463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:37193196..37194477hg38UCSC Ensembl
Outerchr8:37050714..37051995hg19UCSC Ensembl
Outerchr8:37169872..37171153hg18UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg381282
hg191282
hg181282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624587
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)nsv512038
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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