A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512919



Internal ID15852341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:107727212..107727558hg38UCSC Ensembl
Outerchr7:107367657..107368003hg19UCSC Ensembl
Outerchr7:107154893..107155239hg18UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38894
hg19894
hg18894
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625567
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)nsv512919
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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