A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511970



Internal ID15851395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:66392369..66395630hg38UCSC Ensembl
Outerchr7:65857356..65860617hg19UCSC Ensembl
Outerchr7:65494791..65498052hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg383262
hg193262
hg183262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624513
Samples1
Known GenesLINC00174
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511970
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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