A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511868



Internal ID15504607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:31389045..31485555hg38UCSC Ensembl
Outerchr6:31356822..31453332hg19UCSC Ensembl
Outerchr6:31464801..31561311hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3896511
hg1996511
hg1896511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624399
Samples1
Known GenesHCG26, HCP5, MICA
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511868
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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