A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511863



Internal ID15504602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:29977780..29980888hg38UCSC Ensembl
Outerchr6:29945557..29948665hg19UCSC Ensembl
Outerchr6:30053536..30056644hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg383109
hg193109
hg183109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624394
Samples1
Known GenesHCG9
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511863
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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