A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511906



Internal ID15851331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:88090704..88092879hg38UCSC Ensembl
Outerchr6:88800422..88802597hg19UCSC Ensembl
Outerchr6:88857141..88859316hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg382176
hg192176
hg182176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624441
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)nsv511906
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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