A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511363



Internal ID15504102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66124629..66126927hg38UCSC Ensembl
Outerchr7:66122550..66132354hg38UCSC Ensembl
Innerchr7:65589616..65591914hg19UCSC Ensembl
Outerchr7:65587537..65597341hg19UCSC Ensembl
Innerchr7:65227051..65229349hg18UCSC Ensembl
Outerchr7:65224972..65234776hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg389805
hg199805
hg189805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625936
Samples1
Known GenesCRCP
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511363
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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