A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511910



Internal ID15851335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:107709927..107711301hg38UCSC Ensembl
Outerchr6:108031131..108032505hg19UCSC Ensembl
Outerchr6:108137824..108139198hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381375
hg191375
hg181375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624446
Samples1
Known GenesSCML4
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511910
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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