A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511905



Internal ID15851330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:87574527..87577960hg38UCSC Ensembl
Outerchr6:88284245..88287678hg19UCSC Ensembl
Outerchr6:88340964..88344397hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383434
hg193434
hg183434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624440
Samples1
Known GenesRARS2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511905
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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