A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511858



Internal ID15504597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:24811525..24817742hg38UCSC Ensembl
Outerchr6:24811753..24817970hg19UCSC Ensembl
Outerchr6:24919732..24925949hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg386218
hg196218
hg186218
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624388
Samples1
Known GenesFAM65B
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511858
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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