A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607413



Internal ID16048136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66126094..66134209hg38UCSC Ensembl
Innerchr7:65591081..65599196hg19UCSC Ensembl
Innerchr7:65228516..65236631hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg388116
hg198116
hg188116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11433n54
Supporting Variantsnssv1085678
Samples
Known GenesCRCP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607413
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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